Canonical Allele Identifier: CA390513978

Gene: POMT2

Linked Data

• MyVariant Identifiers: chr14:g.77745140A>G (hg19) ; chr14:g.77278797A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77278797A>G , CM000676.2:g.77278797A>G	GRCh38
NC_000014.8:g.77745140A>G , CM000676.1:g.77745140A>G	GRCh37
NC_000014.7:g.76814893A>G	NCBI36
NG_008897.1:g.47086T>C , LRG_844:g.47086T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555134.2:n.889T>C
ENST00000556394.2:c.1505T>C	ENSP00000451967.2:p.Phe502Ser
ENST00000682128.1:c.265T>C	ENSP00000506976.1:n.265T>C
ENST00000682247.1:c.1953T>C	ENSP00000507213.1:p.Phe651=
ENST00000682395.1:n.2428T>C
ENST00000682459.1:n.1667T>C
ENST00000682467.1:c.1892-289T>C	ENSP00000508062.1:n.1892-289T>C
ENST00000682615.1:n.318T>C
ENST00000682795.1:c.2111T>C	ENSP00000507574.1:p.Phe704Ser
ENST00000682895.1:n.1680T>C
ENST00000682955.1:n.1538T>C
ENST00000683095.1:c.370T>C	ENSP00000508040.1:n.370T>C
ENST00000683188.1:c.2225T>C
ENST00000683380.1:n.1628T>C
ENST00000683828.1:c.1673T>C
ENST00000683907.1:c.229T>C	ENSP00000507754.1:p.Ser77Pro
ENST00000684172.1:c.340T>C	ENSP00000508391.1:n.340T>C
ENST00000684259.1:n.3731T>C
ENST00000684538.1:n.1343T>C
ENST00000684549.1:n.1515T>C
ENST00000261534.9:c.1964T>C MANE Select	ENSP00000261534.4:p.Phe655Ser
ENST00000261534.8:c.1964T>C	ENSP00000261534.4:p.Phe655Ser
ENST00000452340.7:n.2940T>C
ENST00000554767.5:n.2750T>C
ENST00000555710.1:c.325T>C	ENSP00000451730.1:n.325T>C
ENST00000556171.1:c.556T>C
ENST00000556394.1:c.88-289T>C
ENST00000556446.1:n.265T>C
ENST00000602717.5:c.179T>C	ENSP00000487704.1:p.Phe60Ser
NM_013382.5:c.1964T>C , LRG_844t1:c.1964T>C	NP_037514.2:p.Phe655Ser
XM_011536675.1:c.2153T>C	XP_011534977.1:p.Phe718Ser
XM_011536676.1:c.1820T>C	XP_011534978.1:p.Phe607Ser
XM_011536677.1:c.1694T>C	XP_011534979.1:p.Phe565Ser
XM_011536679.1:c.1247T>C	XP_011534981.1:p.Phe416Ser
XR_943416.1:n.2217T>C
XM_011536675.2:c.2153T>C	XP_011534977.1:p.Phe718Ser
XM_011536676.2:c.1820T>C	XP_011534978.1:p.Phe607Ser
XM_011536677.3:c.1694T>C	XP_011534979.1:p.Phe565Ser
XR_001750279.1:n.2250T>C
XR_001750282.1:n.2903T>C
XR_943416.3:n.2215T>C
NM_013382.6:c.1964T>C	NP_037514.2:p.Phe655Ser
NM_013382.7:c.1964T>C MANE Select	NP_037514.2:p.Phe655Ser