Canonical Allele Identifier: CA10641768

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57545572C>T , CM000680.2:g.57545572C>T	GRCh38
NC_000018.9:g.55212804C>T , CM000680.1:g.55212804C>T	GRCh37
NC_000018.8:g.53363802C>T	NCBI36
NG_008175.1:g.46166G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000140.5:c.*5140G>A MANE Select	NP_000131.2:n.*5140G>A
ENST00000262093.11:c.*5140G>A MANE Select	ENSP00000262093.6:n.*5140G>A
NM_000140.3:c.*5140G>A	NP_000131.2:n.*5140G>A
NM_000140.4:c.*5140G>A	NP_000131.2:n.*5140G>A
NM_001012515.2:c.*5140G>A	NP_001012533.1:n.*5140G>A
NM_001012515.3:c.*5140G>A	NP_001012533.1:n.*5140G>A
NM_001012515.4:c.*5140G>A	NP_001012533.1:n.*5140G>A
NM_001371094.1:c.*5140G>A	NP_001358023.1:n.*5140G>A
NM_001371095.1:c.*5140G>A	NP_001358024.1:n.*5140G>A
NM_001374778.1:c.*5140G>A	NP_001361707.1:n.*5140G>A
ENST00000652755.1:c.*5140G>A	ENSP00000498358.1:n.*5140G>A