Canonical Allele Identifier: CA1239745890

Gene: HADHB

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26285595_26285596delinsAC , CM000664.2:g.26285595_26285596delinsAC	GRCh38
NC_000002.11:g.26508463_26508464delinsAC , CM000664.1:g.26508463_26508464delinsAC	GRCh37
NC_000002.10:g.26361967_26361968delinsAC	NCBI36
NG_007294.1:g.45643_45644delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317799.10:c.1389+24_1389+25delinsAC MANE Select	ENSP00000325136.5:n.1389+24_1389+25delinsAC
ENST00000317799.9:c.1389+24_1389+25delinsAC	ENSP00000325136.5:n.1389+24_1389+25delinsAC
ENST00000405867.7:c.1020+24_1020+25delinsAC	ENSP00000385411.3:n.1020+24_1020+25delinsAC
ENST00000494615.1:n.2336+24_2336+25delinsAC
ENST00000537713.5:c.1344+24_1344+25delinsAC	ENSP00000444295.1:n.1344+24_1344+25delinsAC
ENST00000545822.2:c.1323+24_1323+25delinsAC	ENSP00000442665.1:n.1323+24_1323+25delinsAC
NM_000183.2:c.1389+24_1389+25delinsAC	NP_000174.1:n.1389+24_1389+25delinsAC
NM_001281512.1:c.1344+24_1344+25delinsAC	NP_001268441.1:n.1344+24_1344+25delinsAC
NM_001281513.1:c.1323+24_1323+25delinsAC	NP_001268442.1:n.1323+24_1323+25delinsAC
XM_011532803.1:c.1389+24_1389+25delinsAC	XP_011531105.1:n.1389+24_1389+25delinsAC
XM_011532804.1:c.1323+24_1323+25delinsAC	XP_011531106.1:n.1323+24_1323+25delinsAC
XM_024452830.1:c.1359+24_1359+25delinsAC	XP_024308598.1:n.1359+24_1359+25delinsAC
XM_024452831.1:c.1323+24_1323+25delinsAC	XP_024308599.1:n.1323+24_1323+25delinsAC
NM_000183.3:c.1389+24_1389+25delinsAC MANE Select	NP_000174.1:n.1389+24_1389+25delinsAC
NM_001281513.2:c.1323+24_1323+25delinsAC	NP_001268442.1:n.1323+24_1323+25delinsAC
NM_001281512.2:c.1344+24_1344+25delinsAC	NP_001268441.1:n.1344+24_1344+25delinsAC