Canonical Allele Identifier: CA2306045965

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57550759G= , CM000680.2:g.57550759G=	GRCh38
NC_000018.9:g.55217991G= , CM000680.1:g.55217991G=	GRCh37
NC_000018.8:g.53368989G=	NCBI36
NG_008175.1:g.40979C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262093.11:c.1225C= MANE Select	ENSP00000262093.6:p.Pro409=
ENST00000382873.8:c.1009C=	ENSP00000372326.4:p.Pro337=
ENST00000651787.1:n.1331C=
ENST00000652755.1:c.1243C=	ENSP00000498358.1:p.Pro415=
ENST00000262093.9:c.1225C=	ENSP00000262093.5:p.Pro409=
ENST00000382873.7:c.1243C=	ENSP00000372326.3:p.Pro415=
ENST00000585494.5:c.*952C=	ENSP00000465243.1:n.*952C=
NM_000140.3:c.1225C=	NP_000131.2:p.Pro409=
NM_001012515.2:c.1243C=	NP_001012533.1:p.Pro415=
XM_011525881.1:c.1144C=	XP_011524183.1:p.Pro382=
XM_011525882.1:c.1009C=	XP_011524184.1:p.Pro337=
NM_000140.4:c.1225C=	NP_000131.2:p.Pro409=
NM_001012515.3:c.1243C=	NP_001012533.1:p.Pro415=
XM_011525882.2:c.1009C=	XP_011524184.1:p.Pro337=
XM_017025614.2:c.1126C=	XP_016881103.1:p.Pro376=
NM_000140.5:c.1225C= MANE Select	NP_000131.2:p.Pro409=
NM_001012515.4:c.1243C=	NP_001012533.1:p.Pro415=
NM_001371094.1:c.1126C=	NP_001358023.1:p.Pro376=
NM_001371095.1:c.1009C=	NP_001358024.1:p.Pro337=
NM_001374778.1:c.1165C=	NP_001361707.1:p.Pro389=