Canonical Allele Identifier: CA349989677

Gene: SLC40A1

Linked Data

• MyVariant Identifiers: chr2:g.190439924G>C (hg19) ; chr2:g.189575198G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575198G>C , CM000664.2:g.189575198G>C	GRCh38
NC_000002.11:g.190439924G>C , CM000664.1:g.190439924G>C	GRCh37
NC_000002.10:g.190148169G>C	NCBI36
NG_009027.1:g.10614C>G , LRG_837:g.10614C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.234C>G MANE Select	ENSP00000261024.3:p.Ile78Met
ENST00000261024.6:c.234C>G	ENSP00000261024.2:p.Ile78Met
ENST00000418714.1:n.675C>G
ENST00000427241.5:c.234C>G	ENSP00000390005.1:p.Ile78Met
ENST00000479598.5:n.515C>G
NM_014585.5:c.234C>G , LRG_837t1:c.234C>G	NP_055400.1:p.Ile78Met
XM_005246505.1:c.114C>G	XP_005246562.1:p.Ile38Met
XM_005246505.2:c.114C>G	XP_005246562.1:p.Ile38Met
XM_017003938.2:c.114C>G	XP_016859427.1:p.Ile38Met
NM_014585.6:c.234C>G MANE Select	NP_055400.1:p.Ile78Met