Canonical Allele Identifier: CA938622124

Gene: FADS2

Linked Data

• dbSNP Id: rs2067160835
• gnomAD v3: 11-61835048-TCCC-T
• gnomAD v4: 11-61835048-TCCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61835049_61835051del , CM000673.2:g.61835049_61835051del	GRCh38
NC_000011.9:g.61602521_61602523del , CM000673.1:g.61602521_61602523del	GRCh37
NC_000011.8:g.61359097_61359099del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278840.9:c.208-2729_208-2727del MANE Select	ENSP00000278840.4:n.208-2729_208-2727del
ENST00000257261.10:c.142-2729_142-2727del	ENSP00000257261.6:n.142-2729_142-2727del
ENST00000278840.8:c.208-2729_208-2727del	ENSP00000278840.4:n.208-2729_208-2727del
ENST00000517312.5:c.-159-2729_-159-2727del	ENSP00000430225.1:n.-159-2729_-159-2727del
ENST00000518606.5:c.-159-2729_-159-2727del	ENSP00000430054.1:n.-159-2729_-159-2727del
ENST00000521849.5:c.208-2729_208-2727del	ENSP00000431091.1:n.208-2729_208-2727del
ENST00000522056.5:c.115-2729_115-2727del	ENSP00000429500.1:n.115-2729_115-2727del
NM_001281501.1:c.142-2729_142-2727del	NP_001268430.1:n.142-2729_142-2727del
NM_001281502.1:c.115-2729_115-2727del	NP_001268431.1:n.115-2729_115-2727del
NM_004265.3:c.208-2729_208-2727del	NP_004256.1:n.208-2729_208-2727del
XM_011545395.1:c.208-2729_208-2727del	XP_011543697.1:n.208-2729_208-2727del
NM_004265.4:c.208-2729_208-2727del MANE Select	NP_004256.1:n.208-2729_208-2727del