Canonical Allele Identifier: CA855513

Gene: SHISAL2A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.52642912T>C , CM000663.2:g.52642912T>C	GRCh38
NC_000001.10:g.53108584T>C , CM000663.1:g.53108584T>C	GRCh37
NC_000001.9:g.52881172T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001042693.3:c.232T>C MANE Select	NP_001036158.1:p.Phe78Leu
ENST00000517870.2:c.232T>C MANE Select	ENSP00000429726.1:p.Phe78Leu
NM_001042693.1:c.232T>C	NP_001036158.1:p.Phe78Leu
NM_001042693.2:c.232T>C	NP_001036158.1:p.Phe78Leu
NR_135156.1:n.475T>C
NR_135156.2:n.651T>C
NR_135157.1:n.382T>C
NR_135157.2:n.558T>C
ENST00000401050.7:n.425T>C
ENST00000424164.1:n.133T>C
ENST00000440303.5:n.382T>C
ENST00000517870.1:c.232T>C	ENSP00000429726.1:p.Phe78Leu
XM_011541377.1:c.244T>C	XP_011539679.1:p.Phe82Leu
XM_011541377.2:c.244T>C	XP_011539679.1:p.Phe82Leu
XM_011541378.1:c.244T>C	XP_011539680.1:p.Phe82Leu
XM_011541378.2:c.244T>C	XP_011539680.1:p.Phe82Leu
XR_946635.1:n.1651T>C
XR_946635.2:n.1652T>C
XR_946636.1:n.1651T>C
XR_946636.2:n.1652T>C
XR_946637.1:n.382T>C
XR_946638.1:n.382T>C
XR_946639.1:n.418T>C
XR_946639.2:n.640T>C