Canonical Allele Identifier: CA1074901930

Gene: SLC45A2

Linked Data

• gnomAD v3: 5-33955642-TACAC-T
• gnomAD v4: 5-33955642-TACAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.33955654_33955657del , CM000667.2:g.33955654_33955657del	GRCh38
NC_000005.9:g.33955759_33955762del , CM000667.1:g.33955759_33955762del	GRCh37
NC_000005.8:g.33991516_33991519del	NCBI36
NG_011691.2:g.34030_34033del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296589.9:c.889-1142_889-1139del MANE Select	ENSP00000296589.4:n.889-1142_889-1139del
ENST00000296589.8:c.889-1142_889-1139del	ENSP00000296589.4:n.889-1142_889-1139del
ENST00000382102.7:c.889-1142_889-1139del	ENSP00000371534.3:n.889-1142_889-1139del
ENST00000509381.1:c.563-1142_563-1139del	ENSP00000421100.1:n.563-1142_563-1139del
ENST00000510600.1:c.364-1142_364-1139del	ENSP00000424010.1:n.364-1142_364-1139del
NM_001012509.3:c.889-1142_889-1139del	NP_001012527.1:n.889-1142_889-1139del
NM_001297417.2:c.563-1142_563-1139del	NP_001284346.2:n.563-1142_563-1139del
NM_016180.4:c.889-1142_889-1139del	NP_057264.3:n.889-1142_889-1139del
XM_011514051.1:c.487-1142_487-1139del	XP_011512353.1:n.487-1142_487-1139del
XR_925620.1:n.1706-1142_1706-1139del
NM_016180.5:c.889-1142_889-1139del MANE Select	NP_057264.4:n.889-1142_889-1139del
NM_001012509.4:c.889-1142_889-1139del	NP_001012527.2:n.889-1142_889-1139del
NM_001297417.3:c.563-1142_563-1139del	NP_001284346.2:n.563-1142_563-1139del
NM_001297417.4:c.563-1142_563-1139del	NP_001284346.2:n.563-1142_563-1139del