Canonical Allele Identifier: CA1468143405
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73415043A= , CM000666.2:g.73415043A= GRCh38
NC_000004.11:g.74280760A= , CM000666.1:g.74280760A= GRCh37
NC_000004.10:g.74499624A= NCBI36
NG_009291.1:g.15789A=

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.9:c.1067A= MANE Select ENSP00000295897.4:p.Tyr356=
ENST00000295897.8:c.1067A= ENSP00000295897.4:p.Tyr356=
ENST00000401494.7:c.722A= ENSP00000384695.3:p.Tyr241=
ENST00000415165.6:c.491A= ENSP00000401820.2:p.Tyr164=
ENST00000476441.6:c.*346A= ENSP00000423727.1:n.*346A=
ENST00000484992.1:n.387A=
ENST00000503124.5:c.617A= ENSP00000421027.1:p.Tyr206=
ENST00000504043.1:n.70A=
ENST00000505649.5:n.753A=
ENST00000509063.5:c.1067A= ENSP00000422784.1:p.Tyr356=
ENST00000511370.1:c.600A=
ENST00000621085.4:c.491-63A= ENSP00000483421.1:n.491-63A=
ENST00000621628.4:c.487-59A= ENSP00000480485.1:n.487-59A=
NM_000477.5:c.1067A= NP_000468.1:p.Tyr356=
NM_000477.6:c.1067A= NP_000468.1:p.Tyr356=
NM_000477.7:c.1067A= MANE Select NP_000468.1:p.Tyr356=