Canonical Allele Identifier: CA390517762

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77753146T>G (hg19) ; chr14:g.77286803T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77286803T>G , CM000676.2:g.77286803T>G	GRCh38
NC_000014.8:g.77753146T>G , CM000676.1:g.77753146T>G	GRCh37
NC_000014.7:g.76822899T>G	NCBI36
NG_008897.1:g.39080A>C , LRG_844:g.39080A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556394.2:c.814A>C	ENSP00000451967.2:p.Ser272Arg
ENST00000682247.1:c.1273A>C	ENSP00000507213.1:p.Ser425Arg
ENST00000682382.1:c.845A>C
ENST00000682395.1:n.1451A>C
ENST00000682459.1:n.976A>C
ENST00000682467.1:c.1273A>C	ENSP00000508062.1:p.Ser425Arg
ENST00000682706.1:n.50A>C
ENST00000682795.1:c.1273A>C	ENSP00000507574.1:p.Ser425Arg
ENST00000682895.1:n.989A>C
ENST00000682955.1:n.561A>C
ENST00000683188.1:c.1248A>C
ENST00000683328.1:c.266A>C	ENSP00000508096.1:n.266A>C
ENST00000683380.1:n.937A>C
ENST00000683828.1:c.982A>C
ENST00000684259.1:n.1124A>C
ENST00000684444.1:c.20A>C
ENST00000684549.1:n.824A>C
ENST00000261534.9:c.1273A>C MANE Select	ENSP00000261534.4:p.Ser425Arg
ENST00000261534.8:c.1273A>C	ENSP00000261534.4:p.Ser425Arg
ENST00000452340.7:n.1296A>C
ENST00000553880.5:n.144A>C
ENST00000554767.5:n.2059A>C
ENST00000554884.5:n.265A>C
ENST00000556404.1:n.407A>C
ENST00000556851.1:n.309A>C
ENST00000557675.5:n.363A>C
NM_013382.5:c.1273A>C , LRG_844t1:c.1273A>C	NP_037514.2:p.Ser425Arg
XM_011536675.1:c.1273A>C	XP_011534977.1:p.Ser425Arg
XM_011536676.1:c.940A>C	XP_011534978.1:p.Ser314Arg
XM_011536677.1:c.814A>C	XP_011534979.1:p.Ser272Arg
XM_011536678.1:c.1273A>C	XP_011534980.1:p.Ser425Arg
XM_011536679.1:c.367A>C	XP_011534981.1:p.Ser123Arg
XR_943416.1:n.1476A>C
XM_011536675.2:c.1273A>C	XP_011534977.1:p.Ser425Arg
XM_011536676.2:c.940A>C	XP_011534978.1:p.Ser314Arg
XM_011536677.3:c.814A>C	XP_011534979.1:p.Ser272Arg
XR_001750279.1:n.1473A>C
XR_001750282.1:n.1926A>C
XR_943416.3:n.1474A>C
NM_013382.6:c.1273A>C	NP_037514.2:p.Ser425Arg
NM_013382.7:c.1273A>C MANE Select	NP_037514.2:p.Ser425Arg