Canonical Allele Identifier: CA1872778140

Gene: SUSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.112060841T>A , CM000671.2:g.112060841T>A	GRCh38
NC_000009.11:g.114823121T>A , CM000671.1:g.114823121T>A	GRCh37
NC_000009.10:g.113862942T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374270.8:c.1850+2096A>T MANE Select	ENSP00000363388.4:n.1850+2096A>T
ENST00000355396.7:c.1800+2096A>T
ENST00000374263.7:c.1850+2096A>T	ENSP00000363381.3:n.1850+2096A>T
ENST00000374264.6:c.1850+2096A>T	ENSP00000363382.2:n.1850+2096A>T
ENST00000374270.7:c.1850+2096A>T	ENSP00000363388.3:n.1850+2096A>T
NM_001282640.1:c.1850+2096A>T	NP_001269569.1:n.1850+2096A>T
NM_001282643.1:c.1850+2096A>T	NP_001269572.1:n.1850+2096A>T
NM_022486.4:c.1850+2096A>T	NP_071931.2:n.1850+2096A>T
XM_011518915.1:c.1889+2096A>T	XP_011517217.1:n.1889+2096A>T
XM_011518916.1:c.1889+2096A>T	XP_011517218.1:n.1889+2096A>T
XM_011518917.1:c.1889+2096A>T	XP_011517219.1:n.1889+2096A>T
XM_011518918.1:c.1889+2096A>T	XP_011517220.1:n.1889+2096A>T
XM_011518919.1:c.1733+2096A>T	XP_011517221.1:n.1733+2096A>T
XR_929833.1:n.2174+2096A>T
XR_929834.1:n.2174+2096A>T
XR_929835.1:n.1987+2096A>T
XM_011518915.2:c.1889+2096A>T	XP_011517217.1:n.1889+2096A>T
XM_011518916.3:c.1889+2096A>T	XP_011517218.1:n.1889+2096A>T
XM_011518917.2:c.1889+2096A>T	XP_011517219.1:n.1889+2096A>T
XM_011518918.2:c.1889+2096A>T	XP_011517220.1:n.1889+2096A>T
XM_011518919.2:c.1733+2096A>T	XP_011517221.1:n.1733+2096A>T
XM_017015037.2:c.1889+2096A>T	XP_016870526.1:n.1889+2096A>T
XM_017015038.2:c.1850+2096A>T	XP_016870527.1:n.1850+2096A>T
XM_017015039.2:c.1889+2096A>T	XP_016870528.1:n.1889+2096A>T
XR_929833.2:n.1951+2096A>T
XR_929835.2:n.1764+2096A>T
NM_001282640.2:c.1850+2096A>T	NP_001269569.1:n.1850+2096A>T
NM_022486.5:c.1850+2096A>T MANE Select	NP_071931.2:n.1850+2096A>T
NM_001282643.2:c.1850+2096A>T	NP_001269572.1:n.1850+2096A>T