Canonical Allele Identifier: CA366870101

Gene: ARL4A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.12688829T>C , CM000669.2:g.12688829T>C	GRCh38
NC_000007.13:g.12728454T>C , CM000669.1:g.12728454T>C	GRCh37
NC_000007.12:g.12694979T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005738.5:c.575T>C MANE Select	NP_005729.1:p.Met192Thr
ENST00000651779.1:c.575T>C MANE Select	ENSP00000498350.1:p.Met192Thr
NM_001037164.2:c.575T>C	NP_001032241.1:p.Met192Thr
NM_001037164.3:c.575T>C	NP_001032241.1:p.Met192Thr
NM_001195396.1:c.575T>C	NP_001182325.1:p.Met192Thr
NM_001195396.2:c.575T>C	NP_001182325.1:p.Met192Thr
NM_005738.4:c.575T>C	NP_005729.1:p.Met192Thr
NM_212460.3:c.575T>C	NP_997625.1:p.Met192Thr
NM_212460.4:c.575T>C	NP_997625.1:p.Met192Thr
ENST00000356797.7:c.575T>C	ENSP00000349250.3:p.Met192Thr
ENST00000396662.5:c.575T>C	ENSP00000379897.1:p.Met192Thr
ENST00000396663.2:c.575T>C	ENSP00000379898.1:p.Met192Thr
ENST00000396664.2:c.575T>C	ENSP00000379899.2:p.Met192Thr
ENST00000404894.1:c.575T>C	ENSP00000385236.1:p.Met192Thr