Canonical Allele Identifier: CA390520953

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77772700T>A (hg19) ; chr14:g.77306357T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77306357T>A , CM000676.2:g.77306357T>A	GRCh38
NC_000014.8:g.77772700T>A , CM000676.1:g.77772700T>A	GRCh37
NC_000014.7:g.76842453T>A	NCBI36
NG_008897.1:g.19526A>T , LRG_844:g.19526A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000555675.6:n.147A>T
ENST00000556394.2:c.249-1557A>T	ENSP00000451967.2:n.249-1557A>T
ENST00000556880.6:n.351A>T
ENST00000682247.1:c.418A>T	ENSP00000507213.1:p.Ser140Cys
ENST00000682382.1:c.366A>T
ENST00000682395.1:n.147A>T
ENST00000682459.1:n.102+45A>T
ENST00000682467.1:c.418A>T	ENSP00000508062.1:p.Ser140Cys
ENST00000682795.1:c.418A>T	ENSP00000507574.1:p.Ser140Cys
ENST00000682895.1:n.134A>T
ENST00000682955.1:n.102+45A>T
ENST00000683188.1:c.213A>T
ENST00000683380.1:n.102+45A>T
ENST00000683828.1:c.287A>T
ENST00000684066.1:n.113A>T
ENST00000684102.1:n.164A>T
ENST00000684259.1:n.269A>T
ENST00000684479.1:n.85A>T
ENST00000684549.1:n.147A>T
ENST00000684600.1:c.232A>T
ENST00000684670.1:n.85A>T
ENST00000684746.1:n.115A>T
ENST00000261534.9:c.418A>T MANE Select	ENSP00000261534.4:p.Ser140Cys
ENST00000261534.8:c.418A>T	ENSP00000261534.4:p.Ser140Cys
ENST00000452340.7:n.441A>T
ENST00000553863.5:n.102+45A>T
ENST00000554948.1:c.145A>T	ENSP00000452060.1:p.Ser49Cys
ENST00000555675.5:n.134A>T
ENST00000555788.5:n.252A>T
ENST00000556326.5:c.*84A>T	ENSP00000450630.1:n.*84A>T
ENST00000556880.5:n.351A>T
ENST00000557525.1:n.508A>T
NM_013382.5:c.418A>T , LRG_844t1:c.418A>T	NP_037514.2:p.Ser140Cys
XM_011536675.1:c.418A>T	XP_011534977.1:p.Ser140Cys
XM_011536676.1:c.85A>T	XP_011534978.1:p.Ser29Cys
XM_011536677.1:c.418A>T	XP_011534979.1:p.Ser140Cys
XM_011536678.1:c.418A>T	XP_011534980.1:p.Ser140Cys
XM_011536680.1:c.418A>T	XP_011534982.1:p.Ser140Cys
XR_943416.1:n.621A>T
XM_011536675.2:c.418A>T	XP_011534977.1:p.Ser140Cys
XM_011536676.2:c.85A>T	XP_011534978.1:p.Ser29Cys
XM_011536677.3:c.418A>T	XP_011534979.1:p.Ser140Cys
XR_001750279.1:n.618A>T
XR_001750282.1:n.622A>T
XR_943416.3:n.619A>T
NM_013382.6:c.418A>T	NP_037514.2:p.Ser140Cys
NM_013382.7:c.418A>T MANE Select	NP_037514.2:p.Ser140Cys