Canonical Allele Identifier: CA2306045885

Gene: FECH

Linked Data

• dbSNP Id: rs2050784189

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57550612G>A , CM000680.2:g.57550612G>A	GRCh38
NC_000018.9:g.55217844G>A , CM000680.1:g.55217844G>A	GRCh37
NC_000018.8:g.53368842G>A	NCBI36
NG_008175.1:g.41126C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000262093.11:c.*100C>T MANE Select	ENSP00000262093.6:n.*100C>T
ENST00000382873.8:c.*100C>T	ENSP00000372326.4:n.*100C>T
ENST00000651787.1:n.1478C>T
ENST00000652755.1:c.*100C>T	ENSP00000498358.1:n.*100C>T
ENST00000262093.9:c.*100C>T	ENSP00000262093.5:n.*100C>T
ENST00000382873.7:c.*100C>T	ENSP00000372326.3:n.*100C>T
ENST00000585494.5:c.*1099C>T	ENSP00000465243.1:n.*1099C>T
NM_000140.3:c.*100C>T	NP_000131.2:n.*100C>T
NM_001012515.2:c.*100C>T	NP_001012533.1:n.*100C>T
XM_011525881.1:c.*100C>T	XP_011524183.1:n.*100C>T
XM_011525882.1:c.*100C>T	XP_011524184.1:n.*100C>T
NM_000140.4:c.*100C>T	NP_000131.2:n.*100C>T
NM_001012515.3:c.*100C>T	NP_001012533.1:n.*100C>T
XM_011525882.2:c.*100C>T	XP_011524184.1:n.*100C>T
XM_017025614.2:c.*100C>T	XP_016881103.1:n.*100C>T
NM_000140.5:c.*100C>T MANE Select	NP_000131.2:n.*100C>T
NM_001012515.4:c.*100C>T	NP_001012533.1:n.*100C>T
NM_001371094.1:c.*100C>T	NP_001358023.1:n.*100C>T
NM_001371095.1:c.*100C>T	NP_001358024.1:n.*100C>T
NM_001374778.1:c.*100C>T	NP_001361707.1:n.*100C>T