Canonical Allele Identifier: CA2610806197

Gene: SFR1

Linked Data

• gnomAD v4: 10-104124216-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104124216A>C , CM000672.2:g.104124216A>C	GRCh38
NC_000010.10:g.105883974A>C , CM000672.1:g.105883974A>C	GRCh37
NC_000010.9:g.105873964A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369727.4:c.546+92A>C MANE Select	ENSP00000358742.3:n.546+92A>C
ENST00000369727.3:c.546+92A>C	ENSP00000358742.3:n.546+92A>C
ENST00000369729.7:c.507+92A>C	ENSP00000358744.3:n.507+92A>C
NM_001002759.1:c.546+92A>C	NP_001002759.1:n.546+92A>C
NM_145247.4:c.507+92A>C	NP_660290.3:n.507+92A>C
XM_005269521.2:c.732+92A>C	XP_005269578.1:n.732+92A>C
XM_005269521.3:c.732+92A>C	XP_005269578.1:n.732+92A>C
XM_017015672.1:c.507+92A>C	XP_016871161.1:n.507+92A>C
NM_001002759.2:c.546+92A>C MANE Select	NP_001002759.1:n.546+92A>C
NM_001384829.1:c.507+92A>C	NP_001371758.1:n.507+92A>C
NM_001384830.1:c.507+92A>C	NP_001371759.1:n.507+92A>C
NM_145247.5:c.507+92A>C	NP_660290.3:n.507+92A>C