Canonical Allele Identifier: CA489922701
Gene: SPRED1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.38591613A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38299412A>T , CM000677.2:g.38299412A>T GRCh38
NC_000015.9:g.38591613A>T , CM000677.1:g.38591613A>T GRCh37
NC_000015.8:g.36378905A>T NCBI36
NG_008980.1:g.51562A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.72A>T MANE Select ENSP00000299084.4:p.Arg24=
ENST00000299084.8:c.72A>T ENSP00000299084.4:p.Arg24=
ENST00000561205.1:n.410A>T
ENST00000561317.1:c.9A>T ENSP00000453680.1:p.Arg3=
NM_152594.2:c.72A>T NP_689807.1:p.Arg24=
XM_005254202.2:c.108A>T XP_005254259.1:p.Arg36=
XM_005254203.3:c.-15-22829A>T XP_005254260.1:n.-15-22829A>T
XM_011521288.1:c.9A>T XP_011519590.1:p.Arg3=
XM_011521289.1:c.9A>T XP_011519591.1:p.Arg3=
XM_011521290.1:c.9A>T XP_011519592.1:p.Arg3=
XM_005254202.3:c.108A>T XP_005254259.1:p.Arg36=
XM_011521289.3:c.9A>T XP_011519591.1:p.Arg3=
NM_152594.3:c.72A>T MANE Select NP_689807.1:p.Arg24=