Canonical Allele Identifier: CA2670965561

Gene: ALB

Linked Data

• gnomAD v4: 4-73415005-CAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415007_73415008del , CM000666.2:g.73415007_73415008del	GRCh38
NC_000004.11:g.74280724_74280725del , CM000666.1:g.74280724_74280725del	GRCh37
NC_000004.10:g.74499588_74499589del	NCBI36
NG_009291.1:g.15753_15754del

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1059-28_1059-27del MANE Select	ENSP00000295897.4:n.1059-28_1059-27del
ENST00000295897.8:c.1059-28_1059-27del	ENSP00000295897.4:n.1059-28_1059-27del
ENST00000401494.7:c.714-28_714-27del	ENSP00000384695.3:n.714-28_714-27del
ENST00000415165.6:c.483-28_483-27del	ENSP00000401820.2:n.483-28_483-27del
ENST00000476441.6:c.*338-28_*338-27del	ENSP00000423727.1:n.*338-28_*338-27del
ENST00000484992.1:n.379-28_379-27del
ENST00000503124.5:c.609-28_609-27del	ENSP00000421027.1:n.609-28_609-27del
ENST00000504043.1:n.62-28_62-27del
ENST00000505649.5:n.745-28_745-27del
ENST00000509063.5:c.1059-28_1059-27del	ENSP00000422784.1:n.1059-28_1059-27del
ENST00000511370.1:c.592-28_592-27del
ENST00000621085.4:c.491-99_491-98del	ENSP00000483421.1:n.491-99_491-98del
ENST00000621628.4:c.487-95_487-94del	ENSP00000480485.1:n.487-95_487-94del
NM_000477.5:c.1059-28_1059-27del	NP_000468.1:n.1059-28_1059-27del
NM_000477.6:c.1059-28_1059-27del	NP_000468.1:n.1059-28_1059-27del
NM_000477.7:c.1059-28_1059-27del MANE Select	NP_000468.1:n.1059-28_1059-27del