Canonical Allele Identifier: CA2211602

Gene: SNED1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241065522C>T , CM000664.2:g.241065522C>T	GRCh38
NC_000002.11:g.242004938C>T , CM000664.1:g.242004938C>T	GRCh37
NC_000002.10:g.241653611C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001080437.3:c.2937C>T MANE Select	NP_001073906.1:p.Ser979=
ENST00000310397.13:c.2937C>T MANE Select	ENSP00000308893.8:p.Ser979=
NM_001080437.1:c.2937C>T	NP_001073906.1:p.Ser979=
NM_001080437.2:c.2937C>T	NP_001073906.1:p.Ser979=
ENST00000310397.12:c.2937C>T	ENSP00000308893.8:p.Ser979=
ENST00000342631.7:c.642C>T	ENSP00000342992.7:p.Ser214=
ENST00000401884.5:c.2937C>T	ENSP00000384871.1:p.Ser979=
ENST00000405547.7:c.2937C>T	ENSP00000386007.3:p.Ser979=
ENST00000466618.1:n.775C>T
XM_011510931.1:c.3009C>T	XP_011509233.1:p.Ser1003=
XM_011510931.2:c.3009C>T	XP_011509233.1:p.Ser1003=
XM_011510932.1:c.3009C>T	XP_011509234.1:p.Ser1003=
XM_011510932.2:c.3009C>T	XP_011509234.1:p.Ser1003=
XM_011510933.1:c.3009C>T	XP_011509235.1:p.Ser1003=
XM_011510933.2:c.3009C>T	XP_011509235.1:p.Ser1003=
XM_011510934.1:c.3009C>T	XP_011509236.1:p.Ser1003=
XM_011510934.3:c.3009C>T	XP_011509236.1:p.Ser1003=
XM_011510935.1:c.3009C>T	XP_011509237.1:p.Ser1003=
XM_011510936.1:c.3009C>T	XP_011509238.1:p.Ser1003=
XM_024452784.1:c.3009C>T	XP_024308552.1:p.Ser1003=
XR_001738694.1:n.3255C>T
XR_001738695.1:n.3255C>T
XR_002959254.1:n.3253C>T
XR_002959255.1:n.3021C>T
XR_002959256.1:n.3254C>T
XR_002959257.1:n.3139C>T
XR_002959258.1:n.3029C>T
XR_002959259.1:n.3017C>T
XR_002959260.1:n.2953C>T
XR_002959261.1:n.2809C>T
XR_002959262.1:n.2785C>T
XR_002959263.1:n.2148C>T
XR_427084.2:n.891C>T
XR_922895.1:n.3039C>T
XR_922896.1:n.3025C>T
XR_922897.1:n.3043C>T
XR_922898.1:n.2925C>T
XR_922899.1:n.2830C>T
XR_922900.1:n.2799C>T
XR_922901.1:n.2953C>T