Canonical Allele Identifier: CA365652371

Gene: ARG1 MED23

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131583166T>C , CM000668.2:g.131583166T>C	GRCh38
NC_000006.11:g.131904306T>C , CM000668.1:g.131904306T>C	GRCh37
NC_000006.10:g.131945999T>C	NCBI36
NG_007086.2:g.14942T>C
NG_031860.1:g.50058A>G
NG_031860.2:g.50058A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000045.4:c.665+2T>C (ARG1) MANE Select	NP_000036.2:n.665+2T>C
ENST00000368087.8:c.665+2T>C (ARG1) MANE Select	ENSP00000357066.3:n.665+2T>C
NM_000045.3:c.665+2T>C (ARG1)	NP_000036.2:n.665+2T>C
NM_001244438.1:c.689+2T>C (ARG1)	NP_001231367.1:n.689+2T>C
NM_001244438.2:c.689+2T>C (ARG1)	NP_001231367.1:n.689+2T>C
NM_001270521.1:c.4077+4543A>G (MED23)	NP_001257450.1:n.4077+4543A>G
NM_001270521.2:c.4077+4543A>G (MED23)	NP_001257450.1:n.4077+4543A>G
NM_001369020.1:c.410+2T>C (ARG1)	NP_001355949.1:n.410+2T>C
NM_015979.3:c.4095+4543A>G (MED23)	NP_057063.2:n.4095+4543A>G
NM_015979.4:c.4095+4543A>G (MED23)	NP_057063.2:n.4095+4543A>G
NR_160934.1:n.649+2T>C (ARG1)
ENST00000275196.5:n.649+2T>C (ARG1)
ENST00000354577.8:c.4095+4543A>G (MED23)	ENSP00000346588.4:n.4095+4543A>G
ENST00000356962.2:c.689+2T>C (ARG1)	ENSP00000349446.2:n.689+2T>C
ENST00000368087.7:c.665+2T>C (ARG1)	ENSP00000357066.3:n.665+2T>C
ENST00000640973.1:c.604+63T>C (ARG1)	ENSP00000492623.1:n.604+63T>C
ENST00000672233.1:c.611+2T>C (ARG1)	ENSP00000499826.1:n.611+2T>C
ENST00000673234.1:c.*552+2T>C (ARG1)	ENSP00000499885.1:n.*552+2T>C
ENST00000673427.1:c.410+2T>C (ARG1)	ENSP00000500160.1:n.410+2T>C
XM_011535801.1:c.410+2T>C (ARG1)	XP_011534103.1:n.410+2T>C
XM_011535801.2:c.410+2T>C (ARG1)	XP_011534103.1:n.410+2T>C