Canonical Allele Identifier: CA357235890

Gene: ALB

Linked Data

• gnomAD v4: 4-73406726-G-T
• MyVariant Identifiers: chr4:g.74272443G>T (hg19) ; chr4:g.73406726G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406726G>T , CM000666.2:g.73406726G>T	GRCh38
NC_000004.11:g.74272443G>T , CM000666.1:g.74272443G>T	GRCh37
NC_000004.10:g.74491307G>T	NCBI36
NG_009291.1:g.7472G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.235G>T MANE Select	ENSP00000295897.4:p.Ala79Ser
ENST00000295897.8:c.235G>T	ENSP00000295897.4:p.Ala79Ser
ENST00000401494.7:c.137+1553G>T	ENSP00000384695.3:n.137+1553G>T
ENST00000415165.6:c.137+1553G>T	ENSP00000401820.2:n.137+1553G>T
ENST00000441319.5:c.241G>T	ENSP00000392541.1:p.Ala81Ser
ENST00000476441.6:c.79+2320G>T	ENSP00000423727.1:n.79+2320G>T
ENST00000503124.5:c.-4G>T	ENSP00000421027.1:n.-4G>T
ENST00000509063.5:c.235G>T	ENSP00000422784.1:p.Ala79Ser
ENST00000510166.5:n.271G>T
ENST00000514786.1:n.204G>T
ENST00000515133.5:n.276G>T
ENST00000621085.4:c.235G>T	ENSP00000483421.1:p.Ala79Ser
ENST00000621628.4:c.235G>T	ENSP00000480485.1:p.Ala79Ser
NM_000477.5:c.235G>T	NP_000468.1:p.Ala79Ser
NM_000477.6:c.235G>T	NP_000468.1:p.Ala79Ser
NM_000477.7:c.235G>T MANE Select	NP_000468.1:p.Ala79Ser