Canonical Allele Identifier: CA2751481860

Gene: TMEM182

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102766595A>T , CM000664.2:g.102766595A>T	GRCh38
NC_000002.11:g.103383054A>T , CM000664.1:g.103383054A>T	GRCh37
NC_000002.10:g.102749486A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000412401.3:c.331+2168A>T MANE Select	ENSP00000394178.2:n.331+2168A>T
ENST00000639249.1:c.43+2168A>T	ENSP00000491614.1:n.43+2168A>T
ENST00000640575.2:c.331+2168A>T	ENSP00000492657.2:n.331+2168A>T
ENST00000409173.5:c.202+2168A>T	ENSP00000387184.1:n.202+2168A>T
ENST00000409528.5:c.43+2168A>T	ENSP00000387258.1:n.43+2168A>T
ENST00000412401.2:c.331+2168A>T	ENSP00000394178.2:n.331+2168A>T
ENST00000454536.5:c.202+2168A>T	ENSP00000392106.1:n.202+2168A>T
ENST00000469971.5:n.281+2168A>T
ENST00000486293.1:n.187+2168A>T
ENST00000488134.5:n.267+2168A>T
NM_144632.3:c.331+2168A>T	NP_653233.3:n.331+2168A>T
XM_006712287.1:c.331+2168A>T	XP_006712350.1:n.331+2168A>T
XM_006712288.2:c.331+2168A>T	XP_006712351.1:n.331+2168A>T
XM_011510630.1:c.202+2168A>T	XP_011508932.1:n.202+2168A>T
XM_011510631.1:c.202+2168A>T	XP_011508933.1:n.202+2168A>T
XM_011510632.1:c.331+2168A>T	XP_011508934.1:n.331+2168A>T
XR_427070.1:n.516+2168A>T
NM_001321343.1:c.202+2168A>T	NP_001308272.1:n.202+2168A>T
NM_001321344.1:c.202+2168A>T	NP_001308273.1:n.202+2168A>T
NM_001321345.1:c.43+2168A>T	NP_001308274.1:n.43+2168A>T
NM_001321346.1:c.43+2168A>T	NP_001308275.1:n.43+2168A>T
NM_144632.4:c.331+2168A>T	NP_653233.4:n.331+2168A>T
XM_006712288.3:c.331+2168A>T	XP_006712351.1:n.331+2168A>T
XM_011510632.2:c.331+2168A>T	XP_011508934.1:n.331+2168A>T
XM_017003375.1:c.331+2168A>T	XP_016858864.1:n.331+2168A>T
XM_017003376.1:c.43+2168A>T	XP_016858865.1:n.43+2168A>T
XR_427070.2:n.516+2168A>T
NM_144632.5:c.331+2168A>T MANE Select	NP_653233.5:n.331+2168A>T
NM_001321343.2:c.202+2168A>T	NP_001308272.2:n.202+2168A>T
NM_001321344.2:c.202+2168A>T	NP_001308273.2:n.202+2168A>T
NM_001321345.2:c.43+2168A>T	NP_001308274.2:n.43+2168A>T
NM_001321346.2:c.43+2168A>T	NP_001308275.2:n.43+2168A>T