Canonical Allele Identifier: CA390520136

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77767462A>G (hg19) ; chr14:g.77301119A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77301119A>G , CM000676.2:g.77301119A>G	GRCh38
NC_000014.8:g.77767462A>G , CM000676.1:g.77767462A>G	GRCh37
NC_000014.7:g.76837215A>G	NCBI36
NG_008897.1:g.24764T>C , LRG_844:g.24764T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553863.6:c.240T>C	ENSP00000508202.1:n.240T>C
ENST00000556394.2:c.358-1558T>C	ENSP00000451967.2:n.358-1558T>C
ENST00000557289.2:c.131T>C
ENST00000682247.1:c.787T>C	ENSP00000507213.1:p.Tyr263His
ENST00000682382.1:c.496-2348T>C
ENST00000682395.1:n.516T>C
ENST00000682459.1:n.451T>C
ENST00000682467.1:c.787T>C	ENSP00000508062.1:p.Tyr263His
ENST00000682795.1:c.787T>C	ENSP00000507574.1:p.Tyr263His
ENST00000682895.1:n.503T>C
ENST00000682955.1:n.212-2348T>C
ENST00000683167.1:c.131T>C
ENST00000683188.1:c.343-1558T>C
ENST00000683300.1:c.109+3573T>C	ENSP00000507630.1:n.109+3573T>C
ENST00000683328.1:c.109+3573T>C	ENSP00000508096.1:n.109+3573T>C
ENST00000683380.1:n.451T>C
ENST00000683398.1:c.131T>C
ENST00000683551.1:c.109+1716T>C
ENST00000683828.1:c.526-1558T>C
ENST00000684259.1:n.638T>C
ENST00000684549.1:n.368-1558T>C
ENST00000684554.1:c.131T>C
ENST00000261534.9:c.787T>C MANE Select	ENSP00000261534.4:p.Tyr263His
ENST00000261534.8:c.787T>C	ENSP00000261534.4:p.Tyr263His
ENST00000452340.7:n.810T>C
ENST00000553863.5:n.451T>C
ENST00000554767.5:n.45T>C
ENST00000555675.5:n.503T>C
ENST00000556326.5:c.*453T>C	ENSP00000450630.1:n.*453T>C
ENST00000557289.1:c.56-1558T>C	ENSP00000451115.1:n.56-1558T>C
NM_013382.5:c.787T>C , LRG_844t1:c.787T>C	NP_037514.2:p.Tyr263His
XM_011536675.1:c.787T>C	XP_011534977.1:p.Tyr263His
XM_011536676.1:c.454T>C	XP_011534978.1:p.Tyr152His
XM_011536677.1:c.547+3573T>C	XP_011534979.1:n.547+3573T>C
XM_011536678.1:c.787T>C	XP_011534980.1:p.Tyr263His
XM_011536679.1:c.-90-1558T>C	XP_011534981.1:n.-90-1558T>C
XM_011536680.1:c.787T>C	XP_011534982.1:p.Tyr263His
XR_943416.1:n.990T>C
XM_011536675.2:c.787T>C	XP_011534977.1:p.Tyr263His
XM_011536676.2:c.454T>C	XP_011534978.1:p.Tyr152His
XM_011536677.3:c.547+3573T>C	XP_011534979.1:n.547+3573T>C
XR_001750279.1:n.987T>C
XR_001750282.1:n.991T>C
XR_943416.3:n.988T>C
NM_013382.6:c.787T>C	NP_037514.2:p.Tyr263His
NM_013382.7:c.787T>C MANE Select	NP_037514.2:p.Tyr263His