Canonical Allele Identifier: CA1315653779
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189563566_189563567delinsTA , CM000664.2:g.189563566_189563567delinsTA GRCh38
NC_000002.11:g.190428292_190428293delinsTA , CM000664.1:g.190428292_190428293delinsTA GRCh37
NC_000002.10:g.190136537_190136538delinsTA NCBI36
NG_009027.1:g.22245_22246delinsTA , LRG_837:g.22245_22246delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.1402+17_1402+18delinsTA MANE Select ENSP00000261024.3:n.1402+17_1402+18delinsTA
ENST00000261024.6:c.1402+17_1402+18delinsTA ENSP00000261024.2:n.1402+17_1402+18delinsTA
NM_014585.5:c.1402+17_1402+18delinsTA , LRG_837t1:c.1402+17_1402+18delinsTA NP_055400.1:n.1402+17_1402+18delinsTA
XM_005246505.1:c.1282+17_1282+18delinsTA XP_005246562.1:n.1282+17_1282+18delinsTA
XM_005246505.2:c.1282+17_1282+18delinsTA XP_005246562.1:n.1282+17_1282+18delinsTA
XM_017003938.2:c.1282+17_1282+18delinsTA XP_016859427.1:n.1282+17_1282+18delinsTA
NM_014585.6:c.1402+17_1402+18delinsTA MANE Select NP_055400.1:n.1402+17_1402+18delinsTA