Canonical Allele Identifier: CA838522054

Gene: SDK1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.4150281T>A , CM000669.2:g.4150281T>A	GRCh38
NC_000007.13:g.4189913T>A , CM000669.1:g.4189913T>A	GRCh37
NC_000007.12:g.4156439T>A	NCBI36
NG_051298.1:g.853834T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404826.7:c.4625+818T>A MANE Select	ENSP00000385899.2:n.4625+818T>A
ENST00000389531.7:c.4625+818T>A	ENSP00000374182.3:n.4625+818T>A
ENST00000404826.6:c.4625+818T>A	ENSP00000385899.2:n.4625+818T>A
ENST00000476701.5:n.909+818T>A
ENST00000615806.4:c.4625+818T>A	ENSP00000478062.1:n.4625+818T>A
NM_001079653.1:c.86+818T>A	NP_001073121.1:n.86+818T>A
NM_152744.3:c.4625+818T>A	NP_689957.3:n.4625+818T>A
XM_011515188.1:c.3395+818T>A	XP_011513490.1:n.3395+818T>A
XM_011515189.1:c.3395+818T>A	XP_011513491.1:n.3395+818T>A
XM_011515190.1:c.3395+818T>A	XP_011513492.1:n.3395+818T>A
XM_017011837.1:c.3395+818T>A	XP_016867326.1:n.3395+818T>A
XM_017011838.1:c.3395+818T>A	XP_016867327.1:n.3395+818T>A
XM_017011839.1:c.3395+818T>A	XP_016867328.1:n.3395+818T>A
XM_017011840.1:c.3395+818T>A	XP_016867329.1:n.3395+818T>A
XM_024446683.1:c.3872+818T>A	XP_024302451.1:n.3872+818T>A
XM_024446684.1:c.3872+818T>A	XP_024302452.1:n.3872+818T>A
NM_152744.4:c.4625+818T>A MANE Select	NP_689957.3:n.4625+818T>A
NM_001079653.2:c.86+818T>A	NP_001073121.1:n.86+818T>A