Canonical Allele Identifier: CA263817852

Gene: POMT2

Linked Data

• dbSNP Id: rs370297950
• gnomAD v3: 14-77279130-C-G
• gnomAD v4: 14-77279130-C-G
• MyVariant Identifiers: chr14:g.77745473C>G (hg19) ; chr14:g.77279130C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77279130C>G , CM000676.2:g.77279130C>G	GRCh38
NC_000014.8:g.77745473C>G , CM000676.1:g.77745473C>G	GRCh37
NC_000014.7:g.76815226C>G	NCBI36
NG_008897.1:g.46753G>C , LRG_844:g.46753G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555134.2:n.817-261G>C
ENST00000556394.2:c.1433-261G>C	ENSP00000451967.2:n.1433-261G>C
ENST00000682128.1:c.193-261G>C	ENSP00000506976.1:n.193-261G>C
ENST00000682247.1:c.1892-272G>C	ENSP00000507213.1:n.1892-272G>C
ENST00000682395.1:n.2356-261G>C
ENST00000682459.1:n.1595-261G>C
ENST00000682467.1:c.1892-622G>C	ENSP00000508062.1:n.1892-622G>C
ENST00000682615.1:n.246-261G>C
ENST00000682795.1:c.2039-261G>C	ENSP00000507574.1:n.2039-261G>C
ENST00000682895.1:n.1608-261G>C
ENST00000682955.1:n.1466-261G>C
ENST00000683095.1:c.298-261G>C	ENSP00000508040.1:n.298-261G>C
ENST00000683188.1:c.2153-261G>C
ENST00000683380.1:n.1556-261G>C
ENST00000683828.1:c.1601-261G>C
ENST00000683907.1:c.157-261G>C	ENSP00000507754.1:n.157-261G>C
ENST00000684172.1:c.268-261G>C	ENSP00000508391.1:n.268-261G>C
ENST00000684259.1:n.3398G>C
ENST00000684538.1:n.1010G>C
ENST00000684549.1:n.1443-261G>C
ENST00000261534.9:c.1892-261G>C MANE Select	ENSP00000261534.4:n.1892-261G>C
ENST00000261534.8:c.1892-261G>C	ENSP00000261534.4:n.1892-261G>C
ENST00000452340.7:n.2607G>C
ENST00000554767.5:n.2678-261G>C
ENST00000555134.1:n.817-261G>C
ENST00000555710.1:c.161-169G>C	ENSP00000451730.1:n.161-169G>C
ENST00000556171.1:c.484-261G>C
ENST00000556394.1:c.88-622G>C
ENST00000602717.5:c.107-261G>C	ENSP00000487704.1:n.107-261G>C
NM_013382.5:c.1892-261G>C , LRG_844t1:c.1892-261G>C	NP_037514.2:n.1892-261G>C
XM_011536675.1:c.2081-261G>C	XP_011534977.1:n.2081-261G>C
XM_011536676.1:c.1748-261G>C	XP_011534978.1:n.1748-261G>C
XM_011536677.1:c.1622-261G>C	XP_011534979.1:n.1622-261G>C
XM_011536678.1:c.*368G>C	XP_011534980.1:n.*368G>C
XM_011536679.1:c.1175-261G>C	XP_011534981.1:n.1175-261G>C
XR_943416.1:n.2145-261G>C
XM_011536675.2:c.2081-261G>C	XP_011534977.1:n.2081-261G>C
XM_011536676.2:c.1748-261G>C	XP_011534978.1:n.1748-261G>C
XM_011536677.3:c.1622-261G>C	XP_011534979.1:n.1622-261G>C
XR_001750279.1:n.2178-261G>C
XR_001750282.1:n.2831-261G>C
XR_943416.3:n.2143-261G>C
NM_013382.6:c.1892-261G>C	NP_037514.2:n.1892-261G>C
NM_013382.7:c.1892-261G>C MANE Select	NP_037514.2:n.1892-261G>C