Canonical Allele Identifier: CA391931849

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38545414A>C (hg19) ; chr15:g.38253213A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253213A>C , CM000677.2:g.38253213A>C	GRCh38
NC_000015.9:g.38545414A>C , CM000677.1:g.38545414A>C	GRCh37
NC_000015.8:g.36332706A>C	NCBI36
NG_008980.1:g.5363A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.28A>C MANE Select	ENSP00000299084.4:p.Asn10His
ENST00000299084.8:c.28A>C	ENSP00000299084.4:p.Asn10His
ENST00000561205.1:n.366A>C
ENST00000561317.1:c.-100A>C	ENSP00000453680.1:n.-100A>C
NM_152594.2:c.28A>C	NP_689807.1:p.Asn10His
XM_005254202.2:c.28A>C	XP_005254259.1:p.Asn10His
XM_005254203.3:c.-20A>C	XP_005254260.1:n.-20A>C
XM_005254202.3:c.28A>C	XP_005254259.1:p.Asn10His
XR_001751484.1:n.87+354T>G
NM_152594.3:c.28A>C MANE Select	NP_689807.1:p.Asn10His