Canonical Allele Identifier: CA2838210459

Gene: PLB1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.28547420T>C , CM000664.2:g.28547420T>C	GRCh38
NC_000002.11:g.28770287T>C , CM000664.1:g.28770287T>C	GRCh37
NC_000002.10:g.28623791T>C	NCBI36
NG_051297.1:g.63842T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327757.10:c.937-1440T>C MANE Select	ENSP00000330442.5:n.937-1440T>C
ENST00000327757.9:c.937-1440T>C	ENSP00000330442.5:n.937-1440T>C
ENST00000404858.5:c.966-1440T>C
ENST00000422425.6:c.970-1440T>C	ENSP00000416440.2:n.970-1440T>C
NM_001170585.1:c.970-1440T>C	NP_001164056.1:n.970-1440T>C
NM_153021.4:c.937-1440T>C	NP_694566.4:n.937-1440T>C
XM_011532579.1:c.997-1440T>C	XP_011530881.1:n.997-1440T>C
XM_011532580.1:c.970-1440T>C	XP_011530882.1:n.970-1440T>C
XM_011532581.1:c.964-1440T>C	XP_011530883.1:n.964-1440T>C
XM_011532582.1:c.997-1440T>C	XP_011530884.1:n.997-1440T>C
XM_011532583.1:c.997-1440T>C	XP_011530885.1:n.997-1440T>C
XM_011532584.1:c.997-1440T>C	XP_011530886.1:n.997-1440T>C
XM_011532585.1:c.997-1440T>C	XP_011530887.1:n.997-1440T>C
XM_011532586.1:c.997-1440T>C	XP_011530888.1:n.997-1440T>C
XM_011532587.1:c.997-1440T>C	XP_011530889.1:n.997-1440T>C
XM_011532588.1:c.997-1440T>C	XP_011530890.1:n.997-1440T>C
XM_011532589.1:c.997-1440T>C	XP_011530891.1:n.997-1440T>C
XM_011532590.1:c.997-1440T>C	XP_011530892.1:n.997-1440T>C
XM_011532591.1:c.997-1440T>C	XP_011530893.1:n.997-1440T>C
XM_011532592.1:c.814-1440T>C	XP_011530894.1:n.814-1440T>C
XM_011532593.1:c.817-1440T>C	XP_011530895.1:n.817-1440T>C
XM_011532594.1:c.997-1440T>C	XP_011530896.1:n.997-1440T>C
XM_011532595.1:c.997-1440T>C	XP_011530897.1:n.997-1440T>C
XM_011532596.1:c.997-1440T>C	XP_011530898.1:n.997-1440T>C
XM_011532597.1:c.997-1440T>C	XP_011530899.1:n.997-1440T>C
XM_011532598.1:c.997-1440T>C	XP_011530900.1:n.997-1440T>C
XM_011532599.1:c.997-1440T>C	XP_011530901.1:n.997-1440T>C
XM_011532600.1:c.165-52T>C	XP_011530902.1:n.165-52T>C
XM_011532601.1:c.24-52T>C	XP_011530903.1:n.24-52T>C
XM_011532602.1:c.1-1440T>C	XP_011530904.1:n.1-1440T>C
XM_011532603.1:c.1-1440T>C	XP_011530905.1:n.1-1440T>C
XM_011532604.1:c.997-1440T>C	XP_011530906.1:n.997-1440T>C
XM_011532605.1:c.-28-52T>C	XP_011530907.1:n.-28-52T>C
XM_011532606.1:c.997-1440T>C	XP_011530908.1:n.997-1440T>C
XM_011532607.1:c.997-1440T>C	XP_011530909.1:n.997-1440T>C
XM_011532608.1:c.997-1440T>C	XP_011530910.1:n.997-1440T>C
XM_011532609.1:c.-601-1440T>C	XP_011530911.1:n.-601-1440T>C
XM_011532611.1:c.997-1440T>C	XP_011530913.1:n.997-1440T>C
XM_011532612.1:c.997-1440T>C	XP_011530914.1:n.997-1440T>C
XR_939661.1:n.1105-1440T>C
XR_939662.1:n.1105-1440T>C
XR_939663.1:n.1105-1440T>C
XR_939664.1:n.1105-1440T>C
XR_939665.1:n.1105-1440T>C
XR_939666.1:n.1105-1440T>C
XR_939667.1:n.1105-1440T>C
XM_011532579.2:c.997-1440T>C	XP_011530881.1:n.997-1440T>C
XM_011532581.3:c.964-1440T>C	XP_011530883.1:n.964-1440T>C
XM_011532584.3:c.997-1440T>C	XP_011530886.1:n.997-1440T>C
XM_011532588.2:c.997-1440T>C	XP_011530890.1:n.997-1440T>C
XM_011532589.2:c.997-1440T>C	XP_011530891.1:n.997-1440T>C
XM_011532590.2:c.997-1440T>C	XP_011530892.1:n.997-1440T>C
XM_011532591.3:c.997-1440T>C	XP_011530893.1:n.997-1440T>C
XM_011532593.2:c.817-1440T>C	XP_011530895.1:n.817-1440T>C
XM_011532601.3:c.24-52T>C	XP_011530903.1:n.24-52T>C
XM_011532602.2:c.1-1440T>C	XP_011530904.1:n.1-1440T>C
XM_011532603.2:c.1-1440T>C	XP_011530905.1:n.1-1440T>C
XM_011532606.3:c.997-1440T>C	XP_011530908.1:n.997-1440T>C
XM_011532607.2:c.997-1440T>C	XP_011530909.1:n.997-1440T>C
XM_011532608.3:c.997-1440T>C	XP_011530910.1:n.997-1440T>C
XM_011532609.2:c.-601-1440T>C	XP_011530911.1:n.-601-1440T>C
XM_017003432.2:c.970-1440T>C	XP_016858921.1:n.970-1440T>C
XM_017003433.2:c.937-1440T>C	XP_016858922.1:n.937-1440T>C
XM_017003434.1:c.997-1440T>C	XP_016858923.1:n.997-1440T>C
XR_001738646.2:n.1299-1440T>C
XR_001738647.2:n.1307-1440T>C
XR_939663.3:n.1295-1440T>C
NM_153021.5:c.937-1440T>C MANE Select	NP_694566.4:n.937-1440T>C
NM_001170585.2:c.970-1440T>C	NP_001164056.1:n.970-1440T>C