Canonical Allele Identifier: CA2574661911

Gene: SFR1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.104124188_104124189insATG , CM000672.2:g.104124188_104124189insATG	GRCh38
NC_000010.10:g.105883946_105883947insATG , CM000672.1:g.105883946_105883947insATG	GRCh37
NC_000010.9:g.105873936_105873937insATG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369727.4:c.546+64_546+65insATG MANE Select	ENSP00000358742.3:n.546+64_546+65insATG
ENST00000369727.3:c.546+64_546+65insATG	ENSP00000358742.3:n.546+64_546+65insATG
ENST00000369729.7:c.507+64_507+65insATG	ENSP00000358744.3:n.507+64_507+65insATG
NM_001002759.1:c.546+64_546+65insATG	NP_001002759.1:n.546+64_546+65insATG
NM_145247.4:c.507+64_507+65insATG	NP_660290.3:n.507+64_507+65insATG
XM_005269521.2:c.732+64_732+65insATG	XP_005269578.1:n.732+64_732+65insATG
XM_005269521.3:c.732+64_732+65insATG	XP_005269578.1:n.732+64_732+65insATG
XM_017015672.1:c.507+64_507+65insATG	XP_016871161.1:n.507+64_507+65insATG
NM_001002759.2:c.546+64_546+65insATG MANE Select	NP_001002759.1:n.546+64_546+65insATG
NM_001384829.1:c.507+64_507+65insATG	NP_001371758.1:n.507+64_507+65insATG
NM_001384830.1:c.507+64_507+65insATG	NP_001371759.1:n.507+64_507+65insATG
NM_145247.5:c.507+64_507+65insATG	NP_660290.3:n.507+64_507+65insATG