Canonical Allele Identifier: CA1468147977

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419465_73419466delinsGT , CM000666.2:g.73419465_73419466delinsGT	GRCh38
NC_000004.11:g.74285182_74285183delinsGT , CM000666.1:g.74285182_74285183delinsGT	GRCh37
NC_000004.10:g.74504046_74504047delinsGT	NCBI36
NG_009291.1:g.20211_20212delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1653-42_1653-41delinsGT MANE Select	ENSP00000295897.4:n.1653-42_1653-41delinsGT
ENST00000295897.8:c.1653-42_1653-41delinsGT	ENSP00000295897.4:n.1653-42_1653-41delinsGT
ENST00000401494.7:c.1308-42_1308-41delinsGT	ENSP00000384695.3:n.1308-42_1308-41delinsGT
ENST00000415165.6:c.1077-42_1077-41delinsGT	ENSP00000401820.2:n.1077-42_1077-41delinsGT
ENST00000476441.6:c.*932-42_*932-41delinsGT	ENSP00000423727.1:n.*932-42_*932-41delinsGT
ENST00000486939.1:n.307-42_307-41delinsGT
ENST00000503124.5:c.1203-42_1203-41delinsGT	ENSP00000421027.1:n.1203-42_1203-41delinsGT
ENST00000505649.5:n.1200-42_1200-41delinsGT
ENST00000508932.5:n.175+10_175+11delinsGT
ENST00000509063.5:c.1653-42_1653-41delinsGT	ENSP00000422784.1:n.1653-42_1653-41delinsGT
ENST00000511370.1:c.1186-42_1186-41delinsGT
ENST00000621085.4:c.1014-42_1014-41delinsGT	ENSP00000483421.1:n.1014-42_1014-41delinsGT
ENST00000621628.4:c.1014-42_1014-41delinsGT	ENSP00000480485.1:n.1014-42_1014-41delinsGT
NM_000477.5:c.1653-42_1653-41delinsGT	NP_000468.1:n.1653-42_1653-41delinsGT
NM_000477.6:c.1653-42_1653-41delinsGT	NP_000468.1:n.1653-42_1653-41delinsGT
NM_000477.7:c.1653-42_1653-41delinsGT MANE Select	NP_000468.1:n.1653-42_1653-41delinsGT