Canonical Allele Identifier: CA708723996

Gene: POMT2

Linked Data

• dbSNP Id: rs1417681244
• MyVariant Identifiers: chr14:g.77772487C>A (hg19) ; chr14:g.77306144C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77306144C>A , CM000676.2:g.77306144C>A	GRCh38
NC_000014.8:g.77772487C>A , CM000676.1:g.77772487C>A	GRCh37
NC_000014.7:g.76842240C>A	NCBI36
NG_008897.1:g.19739G>T , LRG_844:g.19739G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555675.6:n.360G>T
ENST00000556394.2:c.249-1344G>T	ENSP00000451967.2:n.249-1344G>T
ENST00000556880.6:n.462+102G>T
ENST00000682247.1:c.438+193G>T	ENSP00000507213.1:n.438+193G>T
ENST00000682382.1:c.386+193G>T
ENST00000682395.1:n.167+193G>T
ENST00000682459.1:n.102+258G>T
ENST00000682467.1:c.438+193G>T	ENSP00000508062.1:n.438+193G>T
ENST00000682795.1:c.438+193G>T	ENSP00000507574.1:n.438+193G>T
ENST00000682895.1:n.154+193G>T
ENST00000682955.1:n.102+258G>T
ENST00000683188.1:c.233+193G>T
ENST00000683380.1:n.102+258G>T
ENST00000683828.1:c.307+193G>T
ENST00000684102.1:n.377G>T
ENST00000684259.1:n.289+193G>T
ENST00000684479.1:n.105+193G>T
ENST00000684549.1:n.258+102G>T
ENST00000684600.1:c.252+193G>T
ENST00000684670.1:n.105+193G>T
ENST00000261534.9:c.438+193G>T MANE Select	ENSP00000261534.4:n.438+193G>T
ENST00000261534.8:c.438+193G>T	ENSP00000261534.4:n.438+193G>T
ENST00000452340.7:n.461+193G>T
ENST00000553863.5:n.102+258G>T
ENST00000554948.1:c.165+193G>T	ENSP00000452060.1:n.165+193G>T
ENST00000555675.5:n.154+193G>T
ENST00000555788.5:n.363+102G>T
ENST00000556326.5:c.*104+193G>T	ENSP00000450630.1:n.*104+193G>T
ENST00000556880.5:n.462+102G>T
ENST00000557525.1:n.528+193G>T
NM_013382.5:c.438+193G>T , LRG_844t1:c.438+193G>T	NP_037514.2:n.438+193G>T
XM_011536675.1:c.438+193G>T	XP_011534977.1:n.438+193G>T
XM_011536676.1:c.105+193G>T	XP_011534978.1:n.105+193G>T
XM_011536677.1:c.438+193G>T	XP_011534979.1:n.438+193G>T
XM_011536678.1:c.438+193G>T	XP_011534980.1:n.438+193G>T
XM_011536679.1:c.-200+102G>T	XP_011534981.1:n.-200+102G>T
XM_011536680.1:c.438+193G>T	XP_011534982.1:n.438+193G>T
XR_943416.1:n.641+193G>T
XM_011536675.2:c.438+193G>T	XP_011534977.1:n.438+193G>T
XM_011536676.2:c.105+193G>T	XP_011534978.1:n.105+193G>T
XM_011536677.3:c.438+193G>T	XP_011534979.1:n.438+193G>T
XR_001750279.1:n.638+193G>T
XR_001750282.1:n.642+193G>T
XR_943416.3:n.639+193G>T
NM_013382.6:c.438+193G>T	NP_037514.2:n.438+193G>T
NM_013382.7:c.438+193G>T MANE Select	NP_037514.2:n.438+193G>T