Canonical Allele Identifier: CA798250707

Gene: ALB

Linked Data

• dbSNP Id: rs1178293163
• gnomAD v3: 4-73419936-ATTAAT-A
• gnomAD v4: 4-73419936-ATTAAT-A
• MyVariant Identifiers: chr4:g.74285654_74285658del (hg19) ; chr4:g.73419937_73419941del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419940_73419944del , CM000666.2:g.73419940_73419944del	GRCh38
NC_000004.11:g.74285657_74285661del , CM000666.1:g.74285657_74285661del	GRCh37
NC_000004.10:g.74504521_74504525del	NCBI36
NG_009291.1:g.20686_20690del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1785+301_1785+305del MANE Select	ENSP00000295897.4:n.1785+301_1785+305del
ENST00000295897.8:c.1785+301_1785+305del	ENSP00000295897.4:n.1785+301_1785+305del
ENST00000401494.7:c.1440+301_1440+305del	ENSP00000384695.3:n.1440+301_1440+305del
ENST00000415165.6:c.1209+301_1209+305del	ENSP00000401820.2:n.1209+301_1209+305del
ENST00000476441.6:c.*1064+301_*1064+305del	ENSP00000423727.1:n.*1064+301_*1064+305del
ENST00000495173.1:n.93+301_93+305del
ENST00000503124.5:c.1335+301_1335+305del	ENSP00000421027.1:n.1335+301_1335+305del
ENST00000505649.5:n.1332+301_1332+305del
ENST00000508932.5:n.176-314_176-310del
ENST00000509063.5:c.1785+301_1785+305del	ENSP00000422784.1:n.1785+301_1785+305del
ENST00000511370.1:c.1318+301_1318+305del
ENST00000621085.4:c.1146+301_1146+305del	ENSP00000483421.1:n.1146+301_1146+305del
ENST00000621628.4:c.1146+301_1146+305del	ENSP00000480485.1:n.1146+301_1146+305del
NM_000477.5:c.1785+301_1785+305del	NP_000468.1:n.1785+301_1785+305del
NM_000477.6:c.1785+301_1785+305del	NP_000468.1:n.1785+301_1785+305del
NM_000477.7:c.1785+301_1785+305del MANE Select	NP_000468.1:n.1785+301_1785+305del