Canonical Allele Identifier: CA2148315828

Gene: POMT2

Linked Data

• dbSNP Id: rs1890099692
• gnomAD v4: 14-77279021-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.77279021G>A , CM000676.2:g.77279021G>A	GRCh38
NC_000014.8:g.77745364G>A , CM000676.1:g.77745364G>A	GRCh37
NC_000014.7:g.76815117G>A	NCBI36
NG_008897.1:g.46862C>T , LRG_844:g.46862C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555134.2:n.817-152C>T
ENST00000556394.2:c.1433-152C>T	ENSP00000451967.2:n.1433-152C>T
ENST00000682128.1:c.193-152C>T	ENSP00000506976.1:n.193-152C>T
ENST00000682247.1:c.1892-163C>T	ENSP00000507213.1:n.1892-163C>T
ENST00000682395.1:n.2356-152C>T
ENST00000682459.1:n.1595-152C>T
ENST00000682467.1:c.1892-513C>T	ENSP00000508062.1:n.1892-513C>T
ENST00000682615.1:n.246-152C>T
ENST00000682795.1:c.2039-152C>T	ENSP00000507574.1:n.2039-152C>T
ENST00000682895.1:n.1608-152C>T
ENST00000682955.1:n.1466-152C>T
ENST00000683095.1:c.298-152C>T	ENSP00000508040.1:n.298-152C>T
ENST00000683188.1:c.2153-152C>T
ENST00000683380.1:n.1556-152C>T
ENST00000683828.1:c.1601-152C>T
ENST00000683907.1:c.157-152C>T	ENSP00000507754.1:n.157-152C>T
ENST00000684172.1:c.268-152C>T	ENSP00000508391.1:n.268-152C>T
ENST00000684259.1:n.3507C>T
ENST00000684538.1:n.1119C>T
ENST00000684549.1:n.1443-152C>T
ENST00000261534.9:c.1892-152C>T MANE Select	ENSP00000261534.4:n.1892-152C>T
ENST00000261534.8:c.1892-152C>T	ENSP00000261534.4:n.1892-152C>T
ENST00000452340.7:n.2716C>T
ENST00000554767.5:n.2678-152C>T
ENST00000555134.1:n.817-152C>T
ENST00000555710.1:c.161-60C>T	ENSP00000451730.1:n.161-60C>T
ENST00000556171.1:c.484-152C>T
ENST00000556394.1:c.88-513C>T
ENST00000556446.1:n.41C>T
ENST00000602717.5:c.107-152C>T	ENSP00000487704.1:n.107-152C>T
NM_013382.5:c.1892-152C>T , LRG_844t1:c.1892-152C>T	NP_037514.2:n.1892-152C>T
XM_011536675.1:c.2081-152C>T	XP_011534977.1:n.2081-152C>T
XM_011536676.1:c.1748-152C>T	XP_011534978.1:n.1748-152C>T
XM_011536677.1:c.1622-152C>T	XP_011534979.1:n.1622-152C>T
XM_011536678.1:c.*477C>T	XP_011534980.1:n.*477C>T
XM_011536679.1:c.1175-152C>T	XP_011534981.1:n.1175-152C>T
XR_943416.1:n.2145-152C>T
XM_011536675.2:c.2081-152C>T	XP_011534977.1:n.2081-152C>T
XM_011536676.2:c.1748-152C>T	XP_011534978.1:n.1748-152C>T
XM_011536677.3:c.1622-152C>T	XP_011534979.1:n.1622-152C>T
XR_001750279.1:n.2178-152C>T
XR_001750282.1:n.2831-152C>T
XR_943416.3:n.2143-152C>T
NM_013382.6:c.1892-152C>T	NP_037514.2:n.1892-152C>T
NM_013382.7:c.1892-152C>T MANE Select	NP_037514.2:n.1892-152C>T