Canonical Allele Identifier: CA2024299

Gene: SLC40A1

Linked Data

• dbSNP Id: rs775621068
• ExAC: 2:190440086 C / T
• gnomAD v2: 2-190440086-C-T
• gnomAD v4: 2-189575360-C-T
• MyVariant Identifiers: chr2:g.190440086C>T (hg19) ; chr2:g.189575360C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575360C>T , CM000664.2:g.189575360C>T	GRCh38
NC_000002.11:g.190440086C>T , CM000664.1:g.190440086C>T	GRCh37
NC_000002.10:g.190148331C>T	NCBI36
NG_009027.1:g.10452G>A , LRG_837:g.10452G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.112-40G>A MANE Select	ENSP00000261024.3:n.112-40G>A
ENST00000261024.6:c.112-40G>A	ENSP00000261024.2:n.112-40G>A
ENST00000418714.1:n.553-40G>A
ENST00000427241.5:c.112-40G>A	ENSP00000390005.1:n.112-40G>A
ENST00000455320.5:c.112-40G>A	ENSP00000413549.1:n.112-40G>A
ENST00000479598.5:n.393-40G>A
NM_014585.5:c.112-40G>A , LRG_837t1:c.112-40G>A	NP_055400.1:n.112-40G>A
XM_005246505.1:c.-9-40G>A	XP_005246562.1:n.-9-40G>A
XM_005246505.2:c.-9-40G>A	XP_005246562.1:n.-9-40G>A
XM_017003938.2:c.-9-40G>A	XP_016859427.1:n.-9-40G>A
NM_014585.6:c.112-40G>A MANE Select	NP_055400.1:n.112-40G>A