Canonical Allele Identifier: CA390517656

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77753100G>T (hg19) ; chr14:g.77286757G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77286757G>T , CM000676.2:g.77286757G>T	GRCh38
NC_000014.8:g.77753100G>T , CM000676.1:g.77753100G>T	GRCh37
NC_000014.7:g.76822853G>T	NCBI36
NG_008897.1:g.39126C>A , LRG_844:g.39126C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556394.2:c.860C>A	ENSP00000451967.2:p.Thr287Asn
ENST00000682247.1:c.1319C>A	ENSP00000507213.1:p.Thr440Asn
ENST00000682382.1:c.891C>A
ENST00000682395.1:n.1497C>A
ENST00000682459.1:n.1022C>A
ENST00000682467.1:c.1319C>A	ENSP00000508062.1:p.Thr440Asn
ENST00000682706.1:n.96C>A
ENST00000682795.1:c.1319C>A	ENSP00000507574.1:p.Thr440Asn
ENST00000682895.1:n.1035C>A
ENST00000682955.1:n.607C>A
ENST00000683188.1:c.1294C>A
ENST00000683328.1:c.312C>A	ENSP00000508096.1:n.312C>A
ENST00000683380.1:n.983C>A
ENST00000683828.1:c.1028C>A
ENST00000684259.1:n.1170C>A
ENST00000684444.1:c.66C>A
ENST00000684549.1:n.870C>A
ENST00000261534.9:c.1319C>A MANE Select	ENSP00000261534.4:p.Thr440Asn
ENST00000261534.8:c.1319C>A	ENSP00000261534.4:p.Thr440Asn
ENST00000452340.7:n.1342C>A
ENST00000553880.5:n.190C>A
ENST00000554767.5:n.2105C>A
ENST00000554884.5:n.311C>A
ENST00000556404.1:n.453C>A
ENST00000556851.1:n.355C>A
ENST00000557675.5:n.409C>A
NM_013382.5:c.1319C>A , LRG_844t1:c.1319C>A	NP_037514.2:p.Thr440Asn
XM_011536675.1:c.1319C>A	XP_011534977.1:p.Thr440Asn
XM_011536676.1:c.986C>A	XP_011534978.1:p.Thr329Asn
XM_011536677.1:c.860C>A	XP_011534979.1:p.Thr287Asn
XM_011536678.1:c.1319C>A	XP_011534980.1:p.Thr440Asn
XM_011536679.1:c.413C>A	XP_011534981.1:p.Thr138Asn
XR_943416.1:n.1522C>A
XM_011536675.2:c.1319C>A	XP_011534977.1:p.Thr440Asn
XM_011536676.2:c.986C>A	XP_011534978.1:p.Thr329Asn
XM_011536677.3:c.860C>A	XP_011534979.1:p.Thr287Asn
XR_001750279.1:n.1519C>A
XR_001750282.1:n.1972C>A
XR_943416.3:n.1520C>A
NM_013382.6:c.1319C>A	NP_037514.2:p.Thr440Asn
NM_013382.7:c.1319C>A MANE Select	NP_037514.2:p.Thr440Asn