Canonical Allele Identifier: CA390519680

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77765041T>A (hg19) ; chr14:g.77298698T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77298698T>A , CM000676.2:g.77298698T>A	GRCh38
NC_000014.8:g.77765041T>A , CM000676.1:g.77765041T>A	GRCh37
NC_000014.7:g.76834794T>A	NCBI36
NG_008897.1:g.27185A>T , LRG_844:g.27185A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556394.2:c.538A>T	ENSP00000451967.2:p.Ile180Phe
ENST00000557289.2:c.295A>T
ENST00000682247.1:c.997A>T	ENSP00000507213.1:p.Ile333Phe
ENST00000682382.1:c.569A>T
ENST00000682395.1:n.726A>T
ENST00000682459.1:n.661A>T
ENST00000682467.1:c.997A>T	ENSP00000508062.1:p.Ile333Phe
ENST00000682795.1:c.997A>T	ENSP00000507574.1:p.Ile333Phe
ENST00000682895.1:n.713A>T
ENST00000682955.1:n.285A>T
ENST00000683188.1:c.523A>T
ENST00000683300.1:c.110-2425A>T	ENSP00000507630.1:n.110-2425A>T
ENST00000683328.1:c.109+5994A>T	ENSP00000508096.1:n.109+5994A>T
ENST00000683380.1:n.661A>T
ENST00000683551.1:c.183A>T
ENST00000683828.1:c.706A>T
ENST00000684259.1:n.848A>T
ENST00000684549.1:n.548A>T
ENST00000684554.1:c.234A>T
ENST00000261534.9:c.997A>T MANE Select	ENSP00000261534.4:p.Ile333Phe
ENST00000261534.8:c.997A>T	ENSP00000261534.4:p.Ile333Phe
ENST00000452340.7:n.1020A>T
ENST00000554767.5:n.1783A>T
ENST00000557289.1:c.236A>T	ENSP00000451115.1:n.236A>T
NM_013382.5:c.997A>T , LRG_844t1:c.997A>T	NP_037514.2:p.Ile333Phe
XM_011536675.1:c.997A>T	XP_011534977.1:p.Ile333Phe
XM_011536676.1:c.664A>T	XP_011534978.1:p.Ile222Phe
XM_011536677.1:c.548-2425A>T	XP_011534979.1:n.548-2425A>T
XM_011536678.1:c.997A>T	XP_011534980.1:p.Ile333Phe
XM_011536679.1:c.91A>T	XP_011534981.1:p.Ile31Phe
XM_011536680.1:c.997A>T	XP_011534982.1:p.Ile333Phe
XR_943416.1:n.1200A>T
XM_011536675.2:c.997A>T	XP_011534977.1:p.Ile333Phe
XM_011536676.2:c.664A>T	XP_011534978.1:p.Ile222Phe
XM_011536677.3:c.548-2425A>T	XP_011534979.1:n.548-2425A>T
XR_001750279.1:n.1197A>T
XR_001750282.1:n.1201A>T
XR_943416.3:n.1198A>T
NM_013382.6:c.997A>T	NP_037514.2:p.Ile333Phe
NM_013382.7:c.997A>T MANE Select	NP_037514.2:p.Ile333Phe