Canonical Allele Identifier: CA1272831824

Gene: FAM178B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96923302T= , CM000664.2:g.96923302T=	GRCh38
NC_000002.11:g.97589039T= , CM000664.1:g.97589039T=	GRCh37
NC_000002.10:g.96952766T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490605.3:c.1287+188A= MANE Select	ENSP00000429896.1:n.1287+188A=
ENST00000478671.6:n.418+188A=
ENST00000490605.2:c.1287+188A=	ENSP00000429896.1:n.1287+188A=
NM_001122646.2:c.1287+188A=	NP_001116118.2:n.1287+188A=
NR_110209.1:n.467-742T=
XM_011511293.1:c.1209+188A=	XP_011509595.1:n.1209+188A=
XM_011511294.1:c.1179+188A=	XP_011509596.1:n.1179+188A=
XM_011511295.1:c.1287+188A=	XP_011509597.1:n.1287+188A=
XM_011511296.1:c.1287+188A=	XP_011509598.1:n.1287+188A=
XM_011511298.1:c.-55+188A=	XP_011509600.1:n.-55+188A=
XM_011511299.1:c.-55+188A=	XP_011509601.1:n.-55+188A=
XR_427090.2:n.1460+188A=
XM_011511294.2:c.1179+188A=	XP_011509596.1:n.1179+188A=
XM_017004263.1:c.1287+188A=	XP_016859752.1:n.1287+188A=
XM_017004264.1:c.1287+188A=	XP_016859753.1:n.1287+188A=
XM_017004265.1:c.1287+188A=	XP_016859754.1:n.1287+188A=
XM_024452949.1:c.-55+188A=	XP_024308717.1:n.-55+188A=
XM_024452950.1:c.-55+188A=	XP_024308718.1:n.-55+188A=
XM_024452951.1:c.-218+188A=	XP_024308719.1:n.-218+188A=
XR_001738764.1:n.1574+188A=
NM_001122646.3:c.1287+188A= MANE Select	NP_001116118.2:n.1287+188A=