Canonical Allele Identifier: CA1315653753
Gene: SLC40A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189563538_189563539delinsCA , CM000664.2:g.189563538_189563539delinsCA GRCh38
NC_000002.11:g.190428264_190428265delinsCA , CM000664.1:g.190428264_190428265delinsCA GRCh37
NC_000002.10:g.190136509_190136510delinsCA NCBI36
NG_009027.1:g.22273_22274delinsTG , LRG_837:g.22273_22274delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261024.7:c.1402+45_1402+46delinsTG MANE Select ENSP00000261024.3:n.1402+45_1402+46delinsTG
ENST00000261024.6:c.1402+45_1402+46delinsTG ENSP00000261024.2:n.1402+45_1402+46delinsTG
NM_014585.5:c.1402+45_1402+46delinsTG , LRG_837t1:c.1402+45_1402+46delinsTG NP_055400.1:n.1402+45_1402+46delinsTG
XM_005246505.1:c.1282+45_1282+46delinsTG XP_005246562.1:n.1282+45_1282+46delinsTG
XM_005246505.2:c.1282+45_1282+46delinsTG XP_005246562.1:n.1282+45_1282+46delinsTG
XM_017003938.2:c.1282+45_1282+46delinsTG XP_016859427.1:n.1282+45_1282+46delinsTG
NM_014585.6:c.1402+45_1402+46delinsTG MANE Select NP_055400.1:n.1402+45_1402+46delinsTG