Canonical Allele Identifier: CA2008684557

Gene: TMEM45B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.129828961C= , CM000673.2:g.129828961C=	GRCh38
NC_000011.9:g.129698856C= , CM000673.1:g.129698856C=	GRCh37
NC_000011.8:g.129204066C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_138788.5:c.-9+13063C= MANE Select	NP_620143.1:n.-9+13063C=
ENST00000281441.8:c.-9+13063C= MANE Select	ENSP00000281441.3:n.-9+13063C=
NM_001331210.1:c.-158-10592C=	NP_001318139.1:n.-158-10592C=
NM_001331210.2:c.-158-10592C=	NP_001318139.1:n.-158-10592C=
NM_001331211.1:c.-64+13063C=	NP_001318140.1:n.-64+13063C=
NM_001331211.2:c.-64+13063C=	NP_001318140.1:n.-64+13063C=
NM_001331212.1:c.-9+708C=	NP_001318141.1:n.-9+708C=
NM_001331212.2:c.-9+708C=	NP_001318141.1:n.-9+708C=
NM_138788.3:c.-9+13063C=	NP_620143.1:n.-9+13063C=
NM_138788.4:c.-9+13063C=	NP_620143.1:n.-9+13063C=
ENST00000281441.7:c.-9+13063C=	ENSP00000281441.3:n.-9+13063C=
ENST00000527754.1:n.143+708C=
ENST00000529381.1:n.28+13063C=
XM_005271400.3:c.-9+708C=	XP_005271457.1:n.-9+708C=
XM_011542586.1:c.-158-10592C=	XP_011540888.1:n.-158-10592C=
XM_011542587.1:c.-9+708C=	XP_011540889.1:n.-9+708C=
XM_011542588.1:c.-64+13063C=	XP_011540890.1:n.-64+13063C=
XM_017017188.1:c.-159+708C=	XP_016872677.1:n.-159+708C=
XM_017017189.1:c.-159+708C=	XP_016872678.1:n.-159+708C=