Canonical Allele Identifier: CA99707299

Gene: ALB

Linked Data

• dbSNP Id: rs75069738
• MyVariant Identifiers: chr4:g.74280842G>T (hg19) ; chr4:g.73415125G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415125G>T , CM000666.2:g.73415125G>T	GRCh38
NC_000004.11:g.74280842G>T , CM000666.1:g.74280842G>T	GRCh37
NC_000004.10:g.74499706G>T	NCBI36
NG_009291.1:g.15871G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1149G>T MANE Select	ENSP00000295897.4:p.Lys383Asn
ENST00000295897.8:c.1149G>T	ENSP00000295897.4:p.Lys383Asn
ENST00000401494.7:c.804G>T	ENSP00000384695.3:p.Lys268Asn
ENST00000415165.6:c.573G>T	ENSP00000401820.2:p.Lys191Asn
ENST00000476441.6:c.*428G>T	ENSP00000423727.1:n.*428G>T
ENST00000484992.1:n.469G>T
ENST00000503124.5:c.699G>T	ENSP00000421027.1:p.Lys233Asn
ENST00000504043.1:n.152G>T
ENST00000505649.5:n.835G>T
ENST00000509063.5:c.1149G>T	ENSP00000422784.1:p.Lys383Asn
ENST00000511370.1:c.682G>T
ENST00000621085.4:c.510G>T	ENSP00000483421.1:p.Lys170Asn
ENST00000621628.4:c.510G>T	ENSP00000480485.1:p.Lys170Asn
NM_000477.5:c.1149G>T	NP_000468.1:p.Lys383Asn
NM_000477.6:c.1149G>T	NP_000468.1:p.Lys383Asn
NM_000477.7:c.1149G>T MANE Select	NP_000468.1:p.Lys383Asn