Canonical Allele Identifier: CA2625845762

Gene: POMT2

Linked Data

• gnomAD v4: 14-77301357-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77301357C>A , CM000676.2:g.77301357C>A	GRCh38
NC_000014.8:g.77767700C>A , CM000676.1:g.77767700C>A	GRCh37
NC_000014.7:g.76837453C>A	NCBI36
NG_008897.1:g.24526G>T , LRG_844:g.24526G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553863.6:c.110-108G>T	ENSP00000508202.1:n.110-108G>T
ENST00000556394.2:c.358-1796G>T	ENSP00000451967.2:n.358-1796G>T
ENST00000556880.6:n.681-108G>T
ENST00000682247.1:c.657-108G>T	ENSP00000507213.1:n.657-108G>T
ENST00000682382.1:c.496-2586G>T
ENST00000682395.1:n.386-108G>T
ENST00000682459.1:n.321-108G>T
ENST00000682467.1:c.657-108G>T	ENSP00000508062.1:n.657-108G>T
ENST00000682795.1:c.657-108G>T	ENSP00000507574.1:n.657-108G>T
ENST00000682895.1:n.373-108G>T
ENST00000682955.1:n.212-2586G>T
ENST00000683188.1:c.343-1796G>T
ENST00000683300.1:c.109+3335G>T	ENSP00000507630.1:n.109+3335G>T
ENST00000683328.1:c.109+3335G>T	ENSP00000508096.1:n.109+3335G>T
ENST00000683380.1:n.321-108G>T
ENST00000683551.1:c.109+1478G>T
ENST00000683828.1:c.525+1478G>T
ENST00000684259.1:n.508-108G>T
ENST00000684549.1:n.368-1796G>T
ENST00000261534.9:c.657-108G>T MANE Select	ENSP00000261534.4:n.657-108G>T
ENST00000261534.8:c.657-108G>T	ENSP00000261534.4:n.657-108G>T
ENST00000452340.7:n.680-108G>T
ENST00000553863.5:n.321-108G>T
ENST00000554948.1:c.384-108G>T	ENSP00000452060.1:n.384-108G>T
ENST00000555675.5:n.373-108G>T
ENST00000556326.5:c.*323-108G>T	ENSP00000450630.1:n.*323-108G>T
ENST00000557289.1:c.56-1796G>T	ENSP00000451115.1:n.56-1796G>T
NM_013382.5:c.657-108G>T , LRG_844t1:c.657-108G>T	NP_037514.2:n.657-108G>T
XM_011536675.1:c.657-108G>T	XP_011534977.1:n.657-108G>T
XM_011536676.1:c.324-108G>T	XP_011534978.1:n.324-108G>T
XM_011536677.1:c.547+3335G>T	XP_011534979.1:n.547+3335G>T
XM_011536678.1:c.657-108G>T	XP_011534980.1:n.657-108G>T
XM_011536679.1:c.-90-1796G>T	XP_011534981.1:n.-90-1796G>T
XM_011536680.1:c.657-108G>T	XP_011534982.1:n.657-108G>T
XR_943416.1:n.860-108G>T
XM_011536675.2:c.657-108G>T	XP_011534977.1:n.657-108G>T
XM_011536676.2:c.324-108G>T	XP_011534978.1:n.324-108G>T
XM_011536677.3:c.547+3335G>T	XP_011534979.1:n.547+3335G>T
XR_001750279.1:n.857-108G>T
XR_001750282.1:n.861-108G>T
XR_943416.3:n.858-108G>T
NM_013382.6:c.657-108G>T	NP_037514.2:n.657-108G>T
NM_013382.7:c.657-108G>T MANE Select	NP_037514.2:n.657-108G>T