Canonical Allele Identifier: CA349988363

Gene: SLC40A1

Linked Data

• COSMIC: COSM5680116
• MyVariant Identifiers: chr2:g.190428898T>A (hg19) ; chr2:g.189564172T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189564172T>A , CM000664.2:g.189564172T>A	GRCh38
NC_000002.11:g.190428898T>A , CM000664.1:g.190428898T>A	GRCh37
NC_000002.10:g.190137143T>A	NCBI36
NG_009027.1:g.21640A>T , LRG_837:g.21640A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.814A>T MANE Select	ENSP00000261024.3:p.Asn272Tyr
ENST00000261024.6:c.814A>T	ENSP00000261024.2:p.Asn272Tyr
NM_014585.5:c.814A>T , LRG_837t1:c.814A>T	NP_055400.1:p.Asn272Tyr
XM_005246505.1:c.694A>T	XP_005246562.1:p.Asn232Tyr
XM_005246505.2:c.694A>T	XP_005246562.1:p.Asn232Tyr
XM_017003938.2:c.694A>T	XP_016859427.1:p.Asn232Tyr
NM_014585.6:c.814A>T MANE Select	NP_055400.1:p.Asn272Tyr