Canonical Allele Identifier: CA390517630

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77753086C>A (hg19) ; chr14:g.77286743C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77286743C>A , CM000676.2:g.77286743C>A	GRCh38
NC_000014.8:g.77753086C>A , CM000676.1:g.77753086C>A	GRCh37
NC_000014.7:g.76822839C>A	NCBI36
NG_008897.1:g.39140G>T , LRG_844:g.39140G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556394.2:c.873+1G>T	ENSP00000451967.2:n.873+1G>T
ENST00000682247.1:c.1332+1G>T	ENSP00000507213.1:n.1332+1G>T
ENST00000682382.1:c.904+1G>T
ENST00000682395.1:n.1510+1G>T
ENST00000682459.1:n.1035+1G>T
ENST00000682467.1:c.1332+1G>T	ENSP00000508062.1:n.1332+1G>T
ENST00000682795.1:c.1332+1G>T	ENSP00000507574.1:n.1332+1G>T
ENST00000682895.1:n.1048+1G>T
ENST00000682955.1:n.620+1G>T
ENST00000683188.1:c.1307+1G>T
ENST00000683380.1:n.996+1G>T
ENST00000683828.1:c.1041+1G>T
ENST00000684259.1:n.1183+1G>T
ENST00000684444.1:c.80G>T
ENST00000684549.1:n.883+1G>T
ENST00000261534.9:c.1332+1G>T MANE Select	ENSP00000261534.4:n.1332+1G>T
ENST00000261534.8:c.1332+1G>T	ENSP00000261534.4:n.1332+1G>T
ENST00000452340.7:n.1355+1G>T
ENST00000553880.5:n.203+1G>T
ENST00000554767.5:n.2118+1G>T
ENST00000554884.5:n.324+1G>T
ENST00000556404.1:n.466+1G>T
ENST00000557675.5:n.422+1G>T
NM_013382.5:c.1332+1G>T , LRG_844t1:c.1332+1G>T	NP_037514.2:n.1332+1G>T
XM_011536675.1:c.1332+1G>T	XP_011534977.1:n.1332+1G>T
XM_011536676.1:c.999+1G>T	XP_011534978.1:n.999+1G>T
XM_011536677.1:c.873+1G>T	XP_011534979.1:n.873+1G>T
XM_011536678.1:c.1332+1G>T	XP_011534980.1:n.1332+1G>T
XM_011536679.1:c.426+1G>T	XP_011534981.1:n.426+1G>T
XR_943416.1:n.1535+1G>T
XM_011536675.2:c.1332+1G>T	XP_011534977.1:n.1332+1G>T
XM_011536676.2:c.999+1G>T	XP_011534978.1:n.999+1G>T
XM_011536677.3:c.873+1G>T	XP_011534979.1:n.873+1G>T
XR_001750279.1:n.1532+1G>T
XR_001750282.1:n.1985+1G>T
XR_943416.3:n.1533+1G>T
NM_013382.6:c.1332+1G>T	NP_037514.2:n.1332+1G>T
NM_013382.7:c.1332+1G>T MANE Select	NP_037514.2:n.1332+1G>T