Canonical Allele Identifier: CA1468148721

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420154_73420155delinsGA , CM000666.2:g.73420154_73420155delinsGA	GRCh38
NC_000004.11:g.74285871_74285872delinsGA , CM000666.1:g.74285871_74285872delinsGA	GRCh37
NC_000004.10:g.74504735_74504736delinsGA	NCBI36
NG_009291.1:g.20900_20901delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1786-100_1786-99delinsGA MANE Select	ENSP00000295897.4:n.1786-100_1786-99delinsGA
ENST00000295897.8:c.1786-100_1786-99delinsGA	ENSP00000295897.4:n.1786-100_1786-99delinsGA
ENST00000401494.7:c.1441-100_1441-99delinsGA	ENSP00000384695.3:n.1441-100_1441-99delinsGA
ENST00000415165.6:c.1210-100_1210-99delinsGA	ENSP00000401820.2:n.1210-100_1210-99delinsGA
ENST00000476441.6:c.*1065-100_*1065-99delinsGA	ENSP00000423727.1:n.*1065-100_*1065-99delinsGA
ENST00000495173.1:n.94-100_94-99delinsGA
ENST00000503124.5:c.1336-100_1336-99delinsGA	ENSP00000421027.1:n.1336-100_1336-99delinsGA
ENST00000505649.5:n.1333-100_1333-99delinsGA
ENST00000508932.5:n.176-100_176-99delinsGA
ENST00000509063.5:c.1785+515_1785+516delinsGA	ENSP00000422784.1:n.1785+515_1785+516delinsGA
ENST00000511370.1:c.1319-100_1319-99delinsGA
ENST00000621085.4:c.1147-100_1147-99delinsGA	ENSP00000483421.1:n.1147-100_1147-99delinsGA
ENST00000621628.4:c.1147-100_1147-99delinsGA	ENSP00000480485.1:n.1147-100_1147-99delinsGA
NM_000477.5:c.1786-100_1786-99delinsGA	NP_000468.1:n.1786-100_1786-99delinsGA
NM_000477.6:c.1786-100_1786-99delinsGA	NP_000468.1:n.1786-100_1786-99delinsGA
NM_000477.7:c.1786-100_1786-99delinsGA MANE Select	NP_000468.1:n.1786-100_1786-99delinsGA