Canonical Allele Identifier: CA2170799280
Gene: SPRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38322165C= , CM000677.2:g.38322165C= GRCh38
NC_000015.9:g.38614366C= , CM000677.1:g.38614366C= GRCh37
NC_000015.8:g.36401658C= NCBI36
NG_008980.1:g.74315C=

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.208-76C= MANE Select ENSP00000299084.4:n.208-76C=
ENST00000299084.8:c.208-76C= ENSP00000299084.4:n.208-76C=
ENST00000561205.1:n.546-76C=
ENST00000561317.1:c.145-76C= ENSP00000453680.1:n.145-76C=
NM_152594.2:c.208-76C= NP_689807.1:n.208-76C=
XM_005254202.2:c.244-76C= XP_005254259.1:n.244-76C=
XM_005254203.3:c.-15-76C= XP_005254260.1:n.-15-76C=
XM_011521288.1:c.145-76C= XP_011519590.1:n.145-76C=
XM_011521289.1:c.145-76C= XP_011519591.1:n.145-76C=
XM_011521290.1:c.145-76C= XP_011519592.1:n.145-76C=
XM_005254202.3:c.244-76C= XP_005254259.1:n.244-76C=
XM_011521289.3:c.145-76C= XP_011519591.1:n.145-76C=
NM_152594.3:c.208-76C= MANE Select NP_689807.1:n.208-76C=