Canonical Allele Identifier: CA391934837
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38351646A>T , CM000677.2:g.38351646A>T GRCh38
NC_000015.9:g.38643847A>T , CM000677.1:g.38643847A>T GRCh37
NC_000015.8:g.36431139A>T NCBI36
NG_008980.1:g.103796A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.1317A>T MANE Select ENSP00000299084.4:p.Lys439Asn
ENST00000299084.8:c.1317A>T ENSP00000299084.4:p.Lys439Asn
NM_152594.2:c.1317A>T NP_689807.1:p.Lys439Asn
XM_005254202.2:c.1353A>T XP_005254259.1:p.Lys451Asn
XM_005254203.3:c.1095A>T XP_005254260.1:p.Lys365Asn
XM_011521288.1:c.1254A>T XP_011519590.1:p.Lys418Asn
XM_011521289.1:c.1254A>T XP_011519591.1:p.Lys418Asn
XM_011521290.1:c.1254A>T XP_011519592.1:p.Lys418Asn
XM_005254202.3:c.1353A>T XP_005254259.1:p.Lys451Asn
XM_011521289.3:c.1254A>T XP_011519591.1:p.Lys418Asn
NM_152594.3:c.1317A>T MANE Select NP_689807.1:p.Lys439Asn