Canonical Allele Identifier: CA410738530

Gene: SCARF2

Linked Data

• gnomAD v4: 22-20425635-G-T
• MyVariant Identifiers: chr22:g.20779925G>T (hg19) ; chr22:g.20425635G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20425635G>T , CM000684.2:g.20425635G>T	GRCh38
NC_000022.10:g.20779925G>T , CM000684.1:g.20779925G>T	GRCh37
NC_000022.9:g.19109925G>T	NCBI36
NG_031868.2:g.17225C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622235.5:c.2341C>A MANE Select	ENSP00000477564.2:p.Leu781Met
ENST00000615031.4:c.2353C>A	ENSP00000479389.1:p.Leu785Met
ENST00000622235.4:c.2341C>A	ENSP00000477564.1:p.Leu781Met
ENST00000623402.1:c.2356C>A	ENSP00000485276.1:p.Leu786Met
NM_153334.6:c.2356C>A	NP_699165.3:p.Leu786Met
NM_182895.4:c.2341C>A	NP_878315.2:p.Leu781Met
NM_153334.7:c.2356C>A	NP_699165.3:p.Leu786Met
NM_182895.5:c.2341C>A MANE Select	NP_878315.2:p.Leu781Met