Canonical Allele Identifier: CA381197616

Gene: SNX15 ARL2-SNX15

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65035645G>T , CM000673.2:g.65035645G>T	GRCh38
NC_000011.9:g.64803117G>T , CM000673.1:g.64803117G>T	GRCh37
NC_000011.8:g.64559693G>T	NCBI36
NG_029947.1:g.13238G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_013306.5:c.646G>T (SNX15) MANE Select	NP_037438.2:p.Asp216Tyr
ENST00000377244.8:c.646G>T (SNX15) MANE Select	ENSP00000366452.3:p.Asp216Tyr
NM_013306.4:c.646G>T (SNX15)	NP_037438.2:p.Asp216Tyr
NM_147777.3:c.646G>T (SNX15)	NP_680086.2:p.Asp216Tyr
NM_147777.4:c.646G>T (SNX15)	NP_680086.2:p.Asp216Tyr
NR_037650.1:n.1300G>T (ARL2-SNX15)
NR_037650.2:n.1253G>T (ARL2-SNX15)
ENST00000301886.3:c.*863G>T (ARL2-SNX15)	ENSP00000476630.1:n.*863G>T
ENST00000352068.5:c.646G>T (SNX15)	ENSP00000316410.5:p.Asp216Tyr
ENST00000377244.7:c.646G>T (SNX15)	ENSP00000366452.3:p.Asp216Tyr
ENST00000526702.1:n.644G>T (SNX15)
ENST00000534637.5:c.634G>T (SNX15)	ENSP00000437277.1:p.Asp212Tyr