Canonical Allele Identifier: CA2233425221

Gene: TMEM231

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75556246C>T , CM000678.2:g.75556246C>T	GRCh38
NC_000016.9:g.75590144C>T , CM000678.1:g.75590144C>T	GRCh37
NC_000016.8:g.74147645C>T	NCBI36
NG_033109.1:g.5041G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001077418.3:c.-37G>A MANE Select	NP_001070886.1:n.-37G>A
ENST00000258173.11:c.-37G>A MANE Select	ENSP00000258173.5:n.-37G>A
NM_001077416.2:c.26G>A	NP_001070884.2:p.Trp9Ter
NM_001077418.2:c.-37G>A	NP_001070886.1:n.-37G>A
NR_074083.1:n.41G>A
NR_074083.2:n.7G>A
ENST00000258173.10:c.-37G>A	ENSP00000258173.5:n.-37G>A
ENST00000561809.1:n.17G>A
ENST00000562410.5:c.-37G>A	ENSP00000454582.1:n.-37G>A
ENST00000688270.1:c.-37G>A	ENSP00000509823.1:n.-37G>A
ENST00000692215.1:n.7G>A
ENST00000693457.1:c.-37G>A	ENSP00000508414.1:n.-37G>A
ENST00000693682.1:c.-37G>A	ENSP00000508670.1:n.-37G>A