Canonical Allele Identifier: CA490206818

Gene: PATL2

Linked Data

• gnomAD v4: 15-44711291-C-A
• MyVariant Identifiers: chr15:g.45003489C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.44711291C>A , CM000677.2:g.44711291C>A	GRCh38
NC_000015.9:g.45003489C>A , CM000677.1:g.45003489C>A	GRCh37
NC_000015.8:g.42790781C>A	NCBI36
NG_012920.1:g.4805C>A
NG_012920.2:g.4815C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682850.1:c.-525G>T MANE Select	ENSP00000508024.1:n.-525G>T
ENST00000558573.1:n.26G>T
XM_011521338.1:c.-525G>T	XP_011519640.1:n.-525G>T
XM_011521339.1:c.-406G>T	XP_011519641.1:n.-406G>T
XM_011521340.1:c.-347G>T	XP_011519642.1:n.-347G>T
XM_011521343.1:c.-609G>T	XP_011519645.1:n.-609G>T
XM_011521345.1:c.-580G>T	XP_011519647.1:n.-580G>T
XM_011521338.3:c.-525G>T	XP_011519640.1:n.-525G>T
XM_011521339.3:c.-406G>T	XP_011519641.1:n.-406G>T
XM_011521340.3:c.-347G>T	XP_011519642.1:n.-347G>T
XM_011521343.3:c.-609G>T	XP_011519645.1:n.-609G>T
XM_011521345.3:c.-580G>T	XP_011519647.1:n.-580G>T
NM_001387260.1:c.-76+41G>T	NP_001374189.1:n.-76+41G>T
NM_001387261.1:c.-347G>T	NP_001374190.1:n.-347G>T
NM_001387262.1:c.-615G>T	NP_001374191.1:n.-615G>T
NM_001387263.1:c.-525G>T MANE Select	NP_001374192.1:n.-525G>T