Canonical Allele Identifier: CA1739128447

Gene: FAM3C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.121393067T= , CM000669.2:g.121393067T=	GRCh38
NC_000007.13:g.121033121T= , CM000669.1:g.121033121T=	GRCh37
NC_000007.12:g.120820357T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014888.3:c.-42+3095A= MANE Select	NP_055703.1:n.-42+3095A=
ENST00000359943.8:c.-42+3095A= MANE Select	ENSP00000353025.3:n.-42+3095A=
NM_001040020.1:c.-42+3135A=	NP_001035109.1:n.-42+3135A=
NM_001040020.2:c.-42+3135A=	NP_001035109.1:n.-42+3135A=
NM_014888.2:c.-42+3095A=	NP_055703.1:n.-42+3095A=
ENST00000359943.7:c.-42+3095A=	ENSP00000353025.3:n.-42+3095A=
ENST00000412653.5:c.-42+3232A=	ENSP00000408636.1:n.-42+3232A=
ENST00000426156.1:c.-188+3095A=	ENSP00000414940.1:n.-188+3095A=
XM_011515736.1:c.-101-140A=	XP_011514038.1:n.-101-140A=
XM_011515736.2:c.-101-140A=	XP_011514038.1:n.-101-140A=
XM_011515737.1:c.-101-140A=	XP_011514039.1:n.-101-140A=
XM_011515737.2:c.-101-140A=	XP_011514039.1:n.-101-140A=