Canonical Allele Identifier: CA349989932

Gene: SLC40A1

Linked Data

• MyVariant Identifiers: chr2:g.189575349del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189575350del , CM000664.2:g.189575350del	GRCh38
NC_000002.11:g.190440076del , CM000664.1:g.190440076del	GRCh37
NC_000002.10:g.190148321del	NCBI36
NG_009027.1:g.10463del , LRG_837:g.10463del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261024.7:c.112-29del MANE Select	ENSP00000261024.3:n.112-29del
ENST00000261024.6:c.112-29del	ENSP00000261024.2:n.112-29del
ENST00000418714.1:n.553-29del
ENST00000427241.5:c.112-29del	ENSP00000390005.1:n.112-29del
ENST00000455320.5:c.112-29del	ENSP00000413549.1:n.112-29del
ENST00000479598.5:n.393-29del
NM_014585.5:c.112-29del , LRG_837t1:c.112-29del	NP_055400.1:n.112-29del
XM_005246505.1:c.-9-29del	XP_005246562.1:n.-9-29del
XM_005246505.2:c.-9-29del	XP_005246562.1:n.-9-29del
XM_017003938.2:c.-9-29del	XP_016859427.1:n.-9-29del
NM_014585.6:c.112-29del MANE Select	NP_055400.1:n.112-29del