Canonical Allele Identifier: CA558967078
Gene: SLC45A2 HGNC NCBI

Linked Data

dbSNP Id: rs372015410

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.33955675_33955676dup , CM000667.2:g.33955675_33955676dup GRCh38
NC_000005.9:g.33955780_33955781dup , CM000667.1:g.33955780_33955781dup GRCh37
NC_000005.8:g.33991537_33991538dup NCBI36
NG_011691.2:g.34016_34017dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000296589.9:c.889-1156_889-1155dup MANE Select ENSP00000296589.4:n.889-1156_889-1155dup
ENST00000296589.8:c.889-1156_889-1155dup ENSP00000296589.4:n.889-1156_889-1155dup
ENST00000382102.7:c.889-1156_889-1155dup ENSP00000371534.3:n.889-1156_889-1155dup
ENST00000509381.1:c.563-1156_563-1155dup ENSP00000421100.1:n.563-1156_563-1155dup
ENST00000510600.1:c.364-1156_364-1155dup ENSP00000424010.1:n.364-1156_364-1155dup
NM_001012509.3:c.889-1156_889-1155dup NP_001012527.1:n.889-1156_889-1155dup
NM_001297417.2:c.563-1156_563-1155dup NP_001284346.2:n.563-1156_563-1155dup
NM_016180.4:c.889-1156_889-1155dup NP_057264.3:n.889-1156_889-1155dup
XM_011514051.1:c.487-1156_487-1155dup XP_011512353.1:n.487-1156_487-1155dup
XR_925620.1:n.1706-1156_1706-1155dup
NM_016180.5:c.889-1156_889-1155dup MANE Select NP_057264.4:n.889-1156_889-1155dup
NM_001012509.4:c.889-1156_889-1155dup NP_001012527.2:n.889-1156_889-1155dup
NM_001297417.3:c.563-1156_563-1155dup NP_001284346.2:n.563-1156_563-1155dup
NM_001297417.4:c.563-1156_563-1155dup NP_001284346.2:n.563-1156_563-1155dup