Canonical Allele Identifier: CA390517668

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77753106T>A (hg19) ; chr14:g.77286763T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77286763T>A , CM000676.2:g.77286763T>A	GRCh38
NC_000014.8:g.77753106T>A , CM000676.1:g.77753106T>A	GRCh37
NC_000014.7:g.76822859T>A	NCBI36
NG_008897.1:g.39120A>T , LRG_844:g.39120A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556394.2:c.854A>T	ENSP00000451967.2:p.Gln285Leu
ENST00000682247.1:c.1313A>T	ENSP00000507213.1:p.Gln438Leu
ENST00000682382.1:c.885A>T
ENST00000682395.1:n.1491A>T
ENST00000682459.1:n.1016A>T
ENST00000682467.1:c.1313A>T	ENSP00000508062.1:p.Gln438Leu
ENST00000682706.1:n.90A>T
ENST00000682795.1:c.1313A>T	ENSP00000507574.1:p.Gln438Leu
ENST00000682895.1:n.1029A>T
ENST00000682955.1:n.601A>T
ENST00000683188.1:c.1288A>T
ENST00000683328.1:c.306A>T	ENSP00000508096.1:n.306A>T
ENST00000683380.1:n.977A>T
ENST00000683828.1:c.1022A>T
ENST00000684259.1:n.1164A>T
ENST00000684444.1:c.60A>T
ENST00000684549.1:n.864A>T
ENST00000261534.9:c.1313A>T MANE Select	ENSP00000261534.4:p.Gln438Leu
ENST00000261534.8:c.1313A>T	ENSP00000261534.4:p.Gln438Leu
ENST00000452340.7:n.1336A>T
ENST00000553880.5:n.184A>T
ENST00000554767.5:n.2099A>T
ENST00000554884.5:n.305A>T
ENST00000556404.1:n.447A>T
ENST00000556851.1:n.349A>T
ENST00000557675.5:n.403A>T
NM_013382.5:c.1313A>T , LRG_844t1:c.1313A>T	NP_037514.2:p.Gln438Leu
XM_011536675.1:c.1313A>T	XP_011534977.1:p.Gln438Leu
XM_011536676.1:c.980A>T	XP_011534978.1:p.Gln327Leu
XM_011536677.1:c.854A>T	XP_011534979.1:p.Gln285Leu
XM_011536678.1:c.1313A>T	XP_011534980.1:p.Gln438Leu
XM_011536679.1:c.407A>T	XP_011534981.1:p.Gln136Leu
XR_943416.1:n.1516A>T
XM_011536675.2:c.1313A>T	XP_011534977.1:p.Gln438Leu
XM_011536676.2:c.980A>T	XP_011534978.1:p.Gln327Leu
XM_011536677.3:c.854A>T	XP_011534979.1:p.Gln285Leu
XR_001750279.1:n.1513A>T
XR_001750282.1:n.1966A>T
XR_943416.3:n.1514A>T
NM_013382.6:c.1313A>T	NP_037514.2:p.Gln438Leu
NM_013382.7:c.1313A>T MANE Select	NP_037514.2:p.Gln438Leu