Canonical Allele Identifier: CA487509317

Gene: POMT2

Linked Data

• gnomAD v4: 14-77278450-C-T
• MyVariant Identifiers: chr14:g.77744793C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77278450C>T , CM000676.2:g.77278450C>T	GRCh38
NC_000014.8:g.77744793C>T , CM000676.1:g.77744793C>T	GRCh37
NC_000014.7:g.76814546C>T	NCBI36
NG_008897.1:g.47433G>A , LRG_844:g.47433G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555134.2:n.1016G>A
ENST00000556394.2:c.1632G>A	ENSP00000451967.2:p.Leu544=
ENST00000682247.1:c.2080G>A	ENSP00000507213.1:p.Gly694Ser
ENST00000682395.1:n.2555G>A
ENST00000682459.1:n.1794G>A
ENST00000682467.1:c.1950G>A	ENSP00000508062.1:p.Leu650=
ENST00000682795.1:c.2238G>A	ENSP00000507574.1:p.Leu746=
ENST00000682895.1:n.1807G>A
ENST00000682955.1:n.1665G>A
ENST00000683188.1:c.2352G>A
ENST00000683380.1:n.1755G>A
ENST00000683907.1:c.356G>A	ENSP00000507754.1:n.356G>A
ENST00000684259.1:n.3858G>A
ENST00000684538.1:n.1470G>A
ENST00000684549.1:n.1642G>A
ENST00000261534.9:c.2091G>A MANE Select	ENSP00000261534.4:p.Leu697=
ENST00000261534.8:c.2091G>A	ENSP00000261534.4:p.Leu697=
ENST00000452340.7:n.3067G>A
ENST00000554767.5:n.2877G>A
ENST00000555710.1:c.452G>A	ENSP00000451730.1:n.452G>A
ENST00000556394.1:c.146G>A
ENST00000556446.1:n.392G>A
ENST00000602717.5:c.306G>A	ENSP00000487704.1:p.Leu102=
NM_013382.5:c.2091G>A , LRG_844t1:c.2091G>A	NP_037514.2:p.Leu697=
XM_011536675.1:c.2280G>A	XP_011534977.1:p.Leu760=
XM_011536676.1:c.1947G>A	XP_011534978.1:p.Leu649=
XM_011536677.1:c.1821G>A	XP_011534979.1:p.Leu607=
XM_011536679.1:c.1374G>A	XP_011534981.1:p.Leu458=
XR_943416.1:n.2344G>A
XM_011536675.2:c.2280G>A	XP_011534977.1:p.Leu760=
XM_011536676.2:c.1947G>A	XP_011534978.1:p.Leu649=
XM_011536677.3:c.1821G>A	XP_011534979.1:p.Leu607=
XR_001750279.1:n.2377G>A
XR_001750282.1:n.3030G>A
XR_943416.3:n.2342G>A
NM_013382.6:c.2091G>A	NP_037514.2:p.Leu697=
NM_013382.7:c.2091G>A MANE Select	NP_037514.2:p.Leu697=