Canonical Allele Identifier: CA391933374

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38351172-G-C
• MyVariant Identifiers: chr15:g.38643373G>C (hg19) ; chr15:g.38351172G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351172G>C , CM000677.2:g.38351172G>C	GRCh38
NC_000015.9:g.38643373G>C , CM000677.1:g.38643373G>C	GRCh37
NC_000015.8:g.36430665G>C	NCBI36
NG_008980.1:g.103322G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.843G>C MANE Select	ENSP00000299084.4:p.Gln281His
ENST00000299084.8:c.843G>C	ENSP00000299084.4:p.Gln281His
NM_152594.2:c.843G>C	NP_689807.1:p.Gln281His
XM_005254202.2:c.879G>C	XP_005254259.1:p.Gln293His
XM_005254203.3:c.621G>C	XP_005254260.1:p.Gln207His
XM_011521288.1:c.780G>C	XP_011519590.1:p.Gln260His
XM_011521289.1:c.780G>C	XP_011519591.1:p.Gln260His
XM_011521290.1:c.780G>C	XP_011519592.1:p.Gln260His
XM_005254202.3:c.879G>C	XP_005254259.1:p.Gln293His
XM_011521289.3:c.780G>C	XP_011519591.1:p.Gln260His
NM_152594.3:c.843G>C MANE Select	NP_689807.1:p.Gln281His