Canonical Allele Identifier: CA391932888

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38641675T>C (hg19) ; chr15:g.38349474T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38349474T>C , CM000677.2:g.38349474T>C	GRCh38
NC_000015.9:g.38641675T>C , CM000677.1:g.38641675T>C	GRCh37
NC_000015.8:g.36428967T>C	NCBI36
NG_008980.1:g.101624T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.635T>C MANE Select	ENSP00000299084.4:p.Val212Ala
ENST00000299084.8:c.635T>C	ENSP00000299084.4:p.Val212Ala
NM_152594.2:c.635T>C	NP_689807.1:p.Val212Ala
XM_005254202.2:c.671T>C	XP_005254259.1:p.Val224Ala
XM_005254203.3:c.413T>C	XP_005254260.1:p.Val138Ala
XM_011521288.1:c.572T>C	XP_011519590.1:p.Val191Ala
XM_011521289.1:c.572T>C	XP_011519591.1:p.Val191Ala
XM_011521290.1:c.572T>C	XP_011519592.1:p.Val191Ala
XM_005254202.3:c.671T>C	XP_005254259.1:p.Val224Ala
XM_011521289.3:c.572T>C	XP_011519591.1:p.Val191Ala
NM_152594.3:c.635T>C MANE Select	NP_689807.1:p.Val212Ala