Canonical Allele Identifier: CA347267101

Gene: ALMS1

Linked Data

• MyVariant Identifiers: chr2:g.73717128C>A (hg19) ; chr2:g.73490001C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73490001C>A , CM000664.2:g.73490001C>A	GRCh38
NC_000002.11:g.73717128C>A , CM000664.1:g.73717128C>A	GRCh37
NC_000002.10:g.73570636C>A	NCBI36
NG_011690.1:g.109249C>A , LRG_741:g.109249C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682565.1:c.7661C>A	ENSP00000507671.1:p.Ser2554Ter
ENST00000682801.1:c.7661C>A	ENSP00000507862.1:p.Ser2554Ter
ENST00000682859.1:c.7661C>A	ENSP00000508222.1:p.Ser2554Ter
ENST00000683791.1:c.1053C>A
ENST00000684460.1:c.5113C>A
ENST00000684548.1:c.7661C>A	ENSP00000507421.1:p.Ser2554Ter
ENST00000684590.1:c.2108C>A	ENSP00000507376.1:p.Ser703Ter
ENST00000684656.1:c.5113C>A
ENST00000613296.6:c.8042C>A MANE Select	ENSP00000482968.1:p.Ser2681Ter
ENST00000651434.1:c.896-29774C>A
ENST00000423048.5:c.2873C>A	ENSP00000399833.1:p.Ser958Ter
ENST00000484298.5:c.7916C>A	ENSP00000478155.1:p.Ser2639Ter
ENST00000613296.4:c.8042C>A	ENSP00000482968.1:p.Ser2681Ter
ENST00000614410.4:c.8042C>A	ENSP00000479094.1:p.Ser2681Ter
ENST00000620466.4:n.1845C>A
NM_015120.4:c.8045C>A , LRG_741t1:c.8045C>A	NP_055935.4:p.Ser2682Ter
NM_001378454.1:c.8042C>A MANE Select	NP_001365383.1:p.Ser2681Ter