Canonical Allele Identifier: CA390517764

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77753147G>T (hg19) ; chr14:g.77286804G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77286804G>T , CM000676.2:g.77286804G>T	GRCh38
NC_000014.8:g.77753147G>T , CM000676.1:g.77753147G>T	GRCh37
NC_000014.7:g.76822900G>T	NCBI36
NG_008897.1:g.39079C>A , LRG_844:g.39079C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556394.2:c.813C>A	ENSP00000451967.2:p.His271Gln
ENST00000682247.1:c.1272C>A	ENSP00000507213.1:p.His424Gln
ENST00000682382.1:c.844C>A
ENST00000682395.1:n.1450C>A
ENST00000682459.1:n.975C>A
ENST00000682467.1:c.1272C>A	ENSP00000508062.1:p.His424Gln
ENST00000682706.1:n.49C>A
ENST00000682795.1:c.1272C>A	ENSP00000507574.1:p.His424Gln
ENST00000682895.1:n.988C>A
ENST00000682955.1:n.560C>A
ENST00000683188.1:c.1247C>A
ENST00000683328.1:c.265C>A	ENSP00000508096.1:n.265C>A
ENST00000683380.1:n.936C>A
ENST00000683828.1:c.981C>A
ENST00000684259.1:n.1123C>A
ENST00000684444.1:c.19C>A
ENST00000684549.1:n.823C>A
ENST00000261534.9:c.1272C>A MANE Select	ENSP00000261534.4:p.His424Gln
ENST00000261534.8:c.1272C>A	ENSP00000261534.4:p.His424Gln
ENST00000452340.7:n.1295C>A
ENST00000553880.5:n.143C>A
ENST00000554767.5:n.2058C>A
ENST00000554884.5:n.264C>A
ENST00000556404.1:n.406C>A
ENST00000556851.1:n.308C>A
ENST00000557675.5:n.362C>A
NM_013382.5:c.1272C>A , LRG_844t1:c.1272C>A	NP_037514.2:p.His424Gln
XM_011536675.1:c.1272C>A	XP_011534977.1:p.His424Gln
XM_011536676.1:c.939C>A	XP_011534978.1:p.His313Gln
XM_011536677.1:c.813C>A	XP_011534979.1:p.His271Gln
XM_011536678.1:c.1272C>A	XP_011534980.1:p.His424Gln
XM_011536679.1:c.366C>A	XP_011534981.1:p.His122Gln
XR_943416.1:n.1475C>A
XM_011536675.2:c.1272C>A	XP_011534977.1:p.His424Gln
XM_011536676.2:c.939C>A	XP_011534978.1:p.His313Gln
XM_011536677.3:c.813C>A	XP_011534979.1:p.His271Gln
XR_001750279.1:n.1472C>A
XR_001750282.1:n.1925C>A
XR_943416.3:n.1473C>A
NM_013382.6:c.1272C>A	NP_037514.2:p.His424Gln
NM_013382.7:c.1272C>A MANE Select	NP_037514.2:p.His424Gln