Canonical Allele Identifier: CA402538894

Gene: FECH

Linked Data

• MyVariant Identifiers: chr18:g.55217981C>G (hg19) ; chr18:g.57550749C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57550749C>G , CM000680.2:g.57550749C>G	GRCh38
NC_000018.9:g.55217981C>G , CM000680.1:g.55217981C>G	GRCh37
NC_000018.8:g.53368979C>G	NCBI36
NG_008175.1:g.40989G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262093.11:c.1235G>C MANE Select	ENSP00000262093.6:p.Arg412Thr
ENST00000382873.8:c.1019G>C	ENSP00000372326.4:p.Arg340Thr
ENST00000651787.1:n.1341G>C
ENST00000652755.1:c.1253G>C	ENSP00000498358.1:p.Arg418Thr
ENST00000262093.9:c.1235G>C	ENSP00000262093.5:p.Arg412Thr
ENST00000382873.7:c.1253G>C	ENSP00000372326.3:p.Arg418Thr
ENST00000585494.5:c.*962G>C	ENSP00000465243.1:n.*962G>C
NM_000140.3:c.1235G>C	NP_000131.2:p.Arg412Thr
NM_001012515.2:c.1253G>C	NP_001012533.1:p.Arg418Thr
XM_011525881.1:c.1154G>C	XP_011524183.1:p.Arg385Thr
XM_011525882.1:c.1019G>C	XP_011524184.1:p.Arg340Thr
NM_000140.4:c.1235G>C	NP_000131.2:p.Arg412Thr
NM_001012515.3:c.1253G>C	NP_001012533.1:p.Arg418Thr
XM_011525882.2:c.1019G>C	XP_011524184.1:p.Arg340Thr
XM_017025614.2:c.1136G>C	XP_016881103.1:p.Arg379Thr
NM_000140.5:c.1235G>C MANE Select	NP_000131.2:p.Arg412Thr
NM_001012515.4:c.1253G>C	NP_001012533.1:p.Arg418Thr
NM_001371094.1:c.1136G>C	NP_001358023.1:p.Arg379Thr
NM_001371095.1:c.1019G>C	NP_001358024.1:p.Arg340Thr
NM_001374778.1:c.1175G>C	NP_001361707.1:p.Arg392Thr