Canonical Allele Identifier: CA2730171303

Gene: POMT2

Linked Data

• dbSNP Id: rs2140163665

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77279155A>G , CM000676.2:g.77279155A>G	GRCh38
NC_000014.8:g.77745498A>G , CM000676.1:g.77745498A>G	GRCh37
NC_000014.7:g.76815251A>G	NCBI36
NG_008897.1:g.46728T>C , LRG_844:g.46728T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555134.2:n.817-286T>C
ENST00000556394.2:c.1433-286T>C	ENSP00000451967.2:n.1433-286T>C
ENST00000682128.1:c.193-286T>C	ENSP00000506976.1:n.193-286T>C
ENST00000682247.1:c.1892-297T>C	ENSP00000507213.1:n.1892-297T>C
ENST00000682395.1:n.2356-286T>C
ENST00000682459.1:n.1595-286T>C
ENST00000682467.1:c.1892-647T>C	ENSP00000508062.1:n.1892-647T>C
ENST00000682615.1:n.246-286T>C
ENST00000682795.1:c.2039-286T>C	ENSP00000507574.1:n.2039-286T>C
ENST00000682895.1:n.1608-286T>C
ENST00000682955.1:n.1466-286T>C
ENST00000683095.1:c.298-286T>C	ENSP00000508040.1:n.298-286T>C
ENST00000683188.1:c.2153-286T>C
ENST00000683380.1:n.1556-286T>C
ENST00000683828.1:c.1601-286T>C
ENST00000683907.1:c.157-286T>C	ENSP00000507754.1:n.157-286T>C
ENST00000684172.1:c.268-286T>C	ENSP00000508391.1:n.268-286T>C
ENST00000684259.1:n.3373T>C
ENST00000684538.1:n.985T>C
ENST00000684549.1:n.1443-286T>C
ENST00000261534.9:c.1892-286T>C MANE Select	ENSP00000261534.4:n.1892-286T>C
ENST00000261534.8:c.1892-286T>C	ENSP00000261534.4:n.1892-286T>C
ENST00000452340.7:n.2582T>C
ENST00000554767.5:n.2678-286T>C
ENST00000555134.1:n.817-286T>C
ENST00000555710.1:c.161-194T>C	ENSP00000451730.1:n.161-194T>C
ENST00000556171.1:c.484-286T>C
ENST00000556394.1:c.88-647T>C
ENST00000602717.5:c.107-286T>C	ENSP00000487704.1:n.107-286T>C
NM_013382.5:c.1892-286T>C , LRG_844t1:c.1892-286T>C	NP_037514.2:n.1892-286T>C
XM_011536675.1:c.2081-286T>C	XP_011534977.1:n.2081-286T>C
XM_011536676.1:c.1748-286T>C	XP_011534978.1:n.1748-286T>C
XM_011536677.1:c.1622-286T>C	XP_011534979.1:n.1622-286T>C
XM_011536678.1:c.*343T>C	XP_011534980.1:n.*343T>C
XM_011536679.1:c.1175-286T>C	XP_011534981.1:n.1175-286T>C
XR_943416.1:n.2145-286T>C
XM_011536675.2:c.2081-286T>C	XP_011534977.1:n.2081-286T>C
XM_011536676.2:c.1748-286T>C	XP_011534978.1:n.1748-286T>C
XM_011536677.3:c.1622-286T>C	XP_011534979.1:n.1622-286T>C
XR_001750279.1:n.2178-286T>C
XR_001750282.1:n.2831-286T>C
XR_943416.3:n.2143-286T>C
NM_013382.6:c.1892-286T>C	NP_037514.2:n.1892-286T>C
NM_013382.7:c.1892-286T>C MANE Select	NP_037514.2:n.1892-286T>C