Canonical Allele Identifier: CA391934514

Gene: SPRED1

Linked Data

• MyVariant Identifiers: chr15:g.38643727G>C (hg19) ; chr15:g.38351526G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351526G>C , CM000677.2:g.38351526G>C	GRCh38
NC_000015.9:g.38643727G>C , CM000677.1:g.38643727G>C	GRCh37
NC_000015.8:g.36431019G>C	NCBI36
NG_008980.1:g.103676G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1197G>C MANE Select	ENSP00000299084.4:p.Lys399Asn
ENST00000299084.8:c.1197G>C	ENSP00000299084.4:p.Lys399Asn
NM_152594.2:c.1197G>C	NP_689807.1:p.Lys399Asn
XM_005254202.2:c.1233G>C	XP_005254259.1:p.Lys411Asn
XM_005254203.3:c.975G>C	XP_005254260.1:p.Lys325Asn
XM_011521288.1:c.1134G>C	XP_011519590.1:p.Lys378Asn
XM_011521289.1:c.1134G>C	XP_011519591.1:p.Lys378Asn
XM_011521290.1:c.1134G>C	XP_011519592.1:p.Lys378Asn
XM_005254202.3:c.1233G>C	XP_005254259.1:p.Lys411Asn
XM_011521289.3:c.1134G>C	XP_011519591.1:p.Lys378Asn
NM_152594.3:c.1197G>C MANE Select	NP_689807.1:p.Lys399Asn