Canonical Allele Identifier: CA487509347

Gene: POMT2

Linked Data

• ClinVar Variation Id: 2951206
• ClinVar RCV Id: RCV003802468
• gnomAD v4: 14-77278459-T-G
• MyVariant Identifiers: chr14:g.77744802T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77278459T>G , CM000676.2:g.77278459T>G	GRCh38
NC_000014.8:g.77744802T>G , CM000676.1:g.77744802T>G	GRCh37
NC_000014.7:g.76814555T>G	NCBI36
NG_008897.1:g.47424A>C , LRG_844:g.47424A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555134.2:n.1007A>C
ENST00000556394.2:c.1623A>C	ENSP00000451967.2:p.Ser541=
ENST00000682247.1:c.2071A>C	ENSP00000507213.1:p.Met691Leu
ENST00000682395.1:n.2546A>C
ENST00000682459.1:n.1785A>C
ENST00000682467.1:c.1941A>C	ENSP00000508062.1:p.Ser647=
ENST00000682795.1:c.2229A>C	ENSP00000507574.1:p.Ser743=
ENST00000682895.1:n.1798A>C
ENST00000682955.1:n.1656A>C
ENST00000683188.1:c.2343A>C
ENST00000683380.1:n.1746A>C
ENST00000683907.1:c.347A>C	ENSP00000507754.1:n.347A>C
ENST00000684259.1:n.3849A>C
ENST00000684538.1:n.1461A>C
ENST00000684549.1:n.1633A>C
ENST00000261534.9:c.2082A>C MANE Select	ENSP00000261534.4:p.Ser694=
ENST00000261534.8:c.2082A>C	ENSP00000261534.4:p.Ser694=
ENST00000452340.7:n.3058A>C
ENST00000554767.5:n.2868A>C
ENST00000555710.1:c.443A>C	ENSP00000451730.1:n.443A>C
ENST00000556394.1:c.137A>C
ENST00000556446.1:n.383A>C
ENST00000602717.5:c.297A>C	ENSP00000487704.1:p.Ser99=
NM_013382.5:c.2082A>C , LRG_844t1:c.2082A>C	NP_037514.2:p.Ser694=
XM_011536675.1:c.2271A>C	XP_011534977.1:p.Ser757=
XM_011536676.1:c.1938A>C	XP_011534978.1:p.Ser646=
XM_011536677.1:c.1812A>C	XP_011534979.1:p.Ser604=
XM_011536679.1:c.1365A>C	XP_011534981.1:p.Ser455=
XR_943416.1:n.2335A>C
XM_011536675.2:c.2271A>C	XP_011534977.1:p.Ser757=
XM_011536676.2:c.1938A>C	XP_011534978.1:p.Ser646=
XM_011536677.3:c.1812A>C	XP_011534979.1:p.Ser604=
XR_001750279.1:n.2368A>C
XR_001750282.1:n.3021A>C
XR_943416.3:n.2333A>C
NM_013382.6:c.2082A>C	NP_037514.2:p.Ser694=
NM_013382.7:c.2082A>C MANE Select	NP_037514.2:p.Ser694=