Canonical Allele Identifier: CA357240553

Gene: ALB

Linked Data

• MyVariant Identifiers: chr4:g.74279179T>C (hg19) ; chr4:g.73413462T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413462T>C , CM000666.2:g.73413462T>C	GRCh38
NC_000004.11:g.74279179T>C , CM000666.1:g.74279179T>C	GRCh37
NC_000004.10:g.74498043T>C	NCBI36
NG_009291.1:g.14208T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.886T>C MANE Select	ENSP00000295897.4:p.Ser296Pro
ENST00000295897.8:c.886T>C	ENSP00000295897.4:p.Ser296Pro
ENST00000401494.7:c.541T>C	ENSP00000384695.3:p.Ser181Pro
ENST00000415165.6:c.310T>C	ENSP00000401820.2:p.Ser104Pro
ENST00000476441.6:c.*165T>C	ENSP00000423727.1:n.*165T>C
ENST00000484992.1:n.206T>C
ENST00000503124.5:c.436T>C	ENSP00000421027.1:p.Ser146Pro
ENST00000505649.5:n.572T>C
ENST00000509063.5:c.886T>C	ENSP00000422784.1:p.Ser296Pro
ENST00000511370.1:c.419T>C
ENST00000621085.4:c.491-1644T>C	ENSP00000483421.1:n.491-1644T>C
ENST00000621628.4:c.487-1640T>C	ENSP00000480485.1:n.487-1640T>C
NM_000477.5:c.886T>C	NP_000468.1:p.Ser296Pro
NM_000477.6:c.886T>C	NP_000468.1:p.Ser296Pro
NM_000477.7:c.886T>C MANE Select	NP_000468.1:p.Ser296Pro