Canonical Allele Identifier: CA402536831

Gene: FECH

Linked Data

• MyVariant Identifiers: chr18:g.55240495C>G (hg19) ; chr18:g.57573263C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57573263C>G , CM000680.2:g.57573263C>G	GRCh38
NC_000018.9:g.55240495C>G , CM000680.1:g.55240495C>G	GRCh37
NC_000018.8:g.53391493C>G	NCBI36
NG_008175.1:g.18475G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000592699.6:c.297G>C	ENSP00000466263.1:p.Met99Ile
ENST00000682485.1:n.409G>C
ENST00000262093.11:c.297G>C MANE Select	ENSP00000262093.6:p.Met99Ile
ENST00000382873.8:c.81G>C	ENSP00000372326.4:p.Met27Ile
ENST00000651787.1:n.403G>C
ENST00000652755.1:c.315G>C	ENSP00000498358.1:p.Met105Ile
ENST00000262093.9:c.297G>C	ENSP00000262093.5:p.Met99Ile
ENST00000382873.7:c.315G>C	ENSP00000372326.3:p.Met105Ile
ENST00000585494.5:c.297G>C	ENSP00000465243.1:p.Met99Ile
ENST00000585699.1:n.249G>C
ENST00000585747.1:c.297G>C	ENSP00000465717.1:p.Met99Ile
ENST00000585878.1:n.349G>C
ENST00000591215.5:c.81G>C	ENSP00000467461.1:p.Met27Ile
ENST00000592111.1:n.298G>C
ENST00000592699.5:c.297G>C	ENSP00000466263.1:p.Met99Ile
NM_000140.3:c.297G>C	NP_000131.2:p.Met99Ile
NM_001012515.2:c.315G>C	NP_001012533.1:p.Met105Ile
XM_011525881.1:c.315G>C	XP_011524183.1:p.Met105Ile
XM_011525882.1:c.81G>C	XP_011524184.1:p.Met27Ile
NM_000140.4:c.297G>C	NP_000131.2:p.Met99Ile
NM_001012515.3:c.315G>C	NP_001012533.1:p.Met105Ile
XM_011525882.2:c.81G>C	XP_011524184.1:p.Met27Ile
XM_017025614.2:c.297G>C	XP_016881103.1:p.Met99Ile
NM_000140.5:c.297G>C MANE Select	NP_000131.2:p.Met99Ile
NM_001012515.4:c.315G>C	NP_001012533.1:p.Met105Ile
NM_001371094.1:c.297G>C	NP_001358023.1:p.Met99Ile
NM_001371095.1:c.81G>C	NP_001358024.1:p.Met27Ile
NM_001374778.1:c.297G>C	NP_001361707.1:p.Met99Ile