Canonical Allele Identifier: CA12546735

Gene: FAM3C

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.121378525C>T , CM000669.2:g.121378525C>T	GRCh38
NC_000007.13:g.121018579C>T , CM000669.1:g.121018579C>T	GRCh37
NC_000007.12:g.120805815C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359943.8:c.118+385G>A MANE Select	ENSP00000353025.3:n.118+385G>A
ENST00000359943.7:c.118+385G>A	ENSP00000353025.3:n.118+385G>A
ENST00000412653.5:c.118+385G>A	ENSP00000408636.1:n.118+385G>A
ENST00000426156.1:c.28+385G>A	ENSP00000414940.1:n.28+385G>A
NM_001040020.1:c.118+385G>A	NP_001035109.1:n.118+385G>A
NM_014888.2:c.118+385G>A	NP_055703.1:n.118+385G>A
XM_011515736.1:c.118+385G>A	XP_011514038.1:n.118+385G>A
XM_011515737.1:c.118+385G>A	XP_011514039.1:n.118+385G>A
XM_011515736.2:c.118+385G>A	XP_011514038.1:n.118+385G>A
XM_011515737.2:c.118+385G>A	XP_011514039.1:n.118+385G>A
NM_014888.3:c.118+385G>A MANE Select	NP_055703.1:n.118+385G>A
NM_001040020.2:c.118+385G>A	NP_001035109.1:n.118+385G>A