Canonical Allele Identifier: CA2170799276
Gene: SPRED1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38322154C= , CM000677.2:g.38322154C= GRCh38
NC_000015.9:g.38614355C= , CM000677.1:g.38614355C= GRCh37
NC_000015.8:g.36401647C= NCBI36
NG_008980.1:g.74304C=

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.208-87C= MANE Select ENSP00000299084.4:n.208-87C=
ENST00000299084.8:c.208-87C= ENSP00000299084.4:n.208-87C=
ENST00000561205.1:n.546-87C=
ENST00000561317.1:c.145-87C= ENSP00000453680.1:n.145-87C=
NM_152594.2:c.208-87C= NP_689807.1:n.208-87C=
XM_005254202.2:c.244-87C= XP_005254259.1:n.244-87C=
XM_005254203.3:c.-15-87C= XP_005254260.1:n.-15-87C=
XM_011521288.1:c.145-87C= XP_011519590.1:n.145-87C=
XM_011521289.1:c.145-87C= XP_011519591.1:n.145-87C=
XM_011521290.1:c.145-87C= XP_011519592.1:n.145-87C=
XM_005254202.3:c.244-87C= XP_005254259.1:n.244-87C=
XM_011521289.3:c.145-87C= XP_011519591.1:n.145-87C=
NM_152594.3:c.208-87C= MANE Select NP_689807.1:n.208-87C=