Canonical Allele Identifier: CA2580848720

Gene: SLC45A4

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.141290216T= , CM000670.2:g.141290216T=	GRCh38
NC_000008.10:g.142300315T= , CM000670.1:g.142300315T=	GRCh37
NC_000008.9:g.142369497T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000517878.6:c.-401+17880A= MANE Select	ENSP00000428137.1:n.-401+17880A=
ENST00000520137.1:c.-339+17880A=	ENSP00000429033.1:n.-339+17880A=
ENST00000521804.1:n.197+17880A=
XM_011517169.1:c.-401+17880A=	XP_011515471.1:n.-401+17880A=
XM_011517170.1:c.-401+9183A=	XP_011515472.1:n.-401+9183A=
XM_011517171.1:c.-401+15649A=	XP_011515473.1:n.-401+15649A=
XM_011517173.1:c.-401+17880A=	XP_011515475.1:n.-401+17880A=
XM_011517175.1:c.52+9183A=	XP_011515477.1:n.52+9183A=
XM_011517176.1:c.-401+17880A=	XP_011515478.1:n.-401+17880A=
XM_011517179.1:c.-339+17880A=	XP_011515481.1:n.-339+17880A=
XR_928719.1:n.574+30A=
XM_011517169.2:c.-401+17880A=	XP_011515471.1:n.-401+17880A=
XM_011517170.2:c.-401+9183A=	XP_011515472.1:n.-401+9183A=
XM_011517171.2:c.-401+15649A=	XP_011515473.1:n.-401+15649A=
XM_011517173.2:c.-401+17880A=	XP_011515475.1:n.-401+17880A=
XM_011517176.2:c.-401+17880A=	XP_011515478.1:n.-401+17880A=
XM_011517179.2:c.-339+17880A=	XP_011515481.1:n.-339+17880A=
XM_017013648.1:c.-401+9183A=	XP_016869137.1:n.-401+9183A=
XM_017013649.1:c.-401+16924A=	XP_016869138.1:n.-401+16924A=
XM_017013650.2:c.52+9183A=	XP_016869139.1:n.52+9183A=
NM_001286646.2:c.-401+17880A= MANE Select	NP_001273575.1:n.-401+17880A=