Canonical Allele Identifier: CA538918024

Gene: SLC40A1

Linked Data

• dbSNP Id: rs1243847470
• gnomAD v2: 2-190440077-A-G
• gnomAD v4: 2-189575351-A-G
• MyVariant Identifiers: chr2:g.190440077A>G (hg19) ; chr2:g.189575351A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575351A>G , CM000664.2:g.189575351A>G	GRCh38
NC_000002.11:g.190440077A>G , CM000664.1:g.190440077A>G	GRCh37
NC_000002.10:g.190148322A>G	NCBI36
NG_009027.1:g.10461T>C , LRG_837:g.10461T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.112-31T>C MANE Select	ENSP00000261024.3:n.112-31T>C
ENST00000261024.6:c.112-31T>C	ENSP00000261024.2:n.112-31T>C
ENST00000418714.1:n.553-31T>C
ENST00000427241.5:c.112-31T>C	ENSP00000390005.1:n.112-31T>C
ENST00000455320.5:c.112-31T>C	ENSP00000413549.1:n.112-31T>C
ENST00000479598.5:n.393-31T>C
NM_014585.5:c.112-31T>C , LRG_837t1:c.112-31T>C	NP_055400.1:n.112-31T>C
XM_005246505.1:c.-9-31T>C	XP_005246562.1:n.-9-31T>C
XM_005246505.2:c.-9-31T>C	XP_005246562.1:n.-9-31T>C
XM_017003938.2:c.-9-31T>C	XP_016859427.1:n.-9-31T>C
NM_014585.6:c.112-31T>C MANE Select	NP_055400.1:n.112-31T>C