Canonical Allele Identifier: CA2658216635

Gene: HADHB

Linked Data

• gnomAD v4: 2-26282931-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26282934del , CM000664.2:g.26282934del	GRCh38
NC_000002.11:g.26505802del , CM000664.1:g.26505802del	GRCh37
NC_000002.10:g.26359306del	NCBI36
NG_007294.1:g.42982del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317799.10:c.1013+10del MANE Select	ENSP00000325136.5:n.1013+10del
ENST00000317799.9:c.1013+10del	ENSP00000325136.5:n.1013+10del
ENST00000405867.7:c.644+10del	ENSP00000385411.3:n.644+10del
ENST00000494615.1:n.1960+10del
ENST00000537713.5:c.968+10del	ENSP00000444295.1:n.968+10del
ENST00000545822.2:c.947+10del	ENSP00000442665.1:n.947+10del
NM_000183.2:c.1013+10del	NP_000174.1:n.1013+10del
NM_001281512.1:c.968+10del	NP_001268441.1:n.968+10del
NM_001281513.1:c.947+10del	NP_001268442.1:n.947+10del
XM_011532803.1:c.1013+10del	XP_011531105.1:n.1013+10del
XM_011532804.1:c.947+10del	XP_011531106.1:n.947+10del
XM_024452830.1:c.983+10del	XP_024308598.1:n.983+10del
XM_024452831.1:c.947+10del	XP_024308599.1:n.947+10del
NM_000183.3:c.1013+10del MANE Select	NP_000174.1:n.1013+10del
NM_001281513.2:c.947+10del	NP_001268442.1:n.947+10del
NM_001281512.2:c.968+10del	NP_001268441.1:n.968+10del