Canonical Allele Identifier: CA2879523

Gene: SLC34A2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25667996G>A , CM000666.2:g.25667996G>A	GRCh38
NC_000004.11:g.25669618G>A , CM000666.1:g.25669618G>A	GRCh37
NC_000004.10:g.25278716G>A	NCBI36
NG_021185.1:g.17184G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006424.3:c.635+5G>A MANE Select	NP_006415.3:n.635+5G>A
ENST00000382051.8:c.635+5G>A MANE Select	ENSP00000371483.3:n.635+5G>A
NM_001177998.1:c.632+5G>A	NP_001171469.1:n.632+5G>A
NM_001177998.2:c.632+5G>A	NP_001171469.2:n.632+5G>A
NM_001177999.1:c.632+5G>A	NP_001171470.1:n.632+5G>A
NM_001177999.2:c.632+5G>A	NP_001171470.2:n.632+5G>A
NM_006424.2:c.635+5G>A	NP_006415.2:n.635+5G>A
ENST00000382051.7:c.635+5G>A	ENSP00000371483.3:n.635+5G>A
ENST00000503434.5:c.632+5G>A	ENSP00000423021.1:n.632+5G>A
ENST00000504570.5:c.632+5G>A	ENSP00000425501.1:n.632+5G>A
ENST00000510033.2:n.653+5G>A
ENST00000645788.1:c.632+5G>A	ENSP00000494094.1:n.632+5G>A