Canonical Allele Identifier: CA102781517

Gene: INTS12 ARHGEF38

Linked Data

• dbSNP Id: rs1050078832
• gnomAD v3: 4-105698029-A-G
• gnomAD v4: 4-105698029-A-G
• MyVariant Identifiers: chr4:g.106619186A>G (hg19) ; chr4:g.105698029A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105698029A>G , CM000666.2:g.105698029A>G	GRCh38
NC_000004.11:g.106619186A>G , CM000666.1:g.106619186A>G	GRCh37
NC_000004.10:g.106838635A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000340139.10:c.156+1821T>C (INTS12) MANE Select	ENSP00000340737.5:n.156+1821T>C
ENST00000340139.9:c.156+1821T>C (INTS12)	ENSP00000340737.5:n.156+1821T>C
ENST00000394735.5:c.156+1821T>C (INTS12)	ENSP00000378221.1:n.156+1821T>C
ENST00000416543.5:c.156+1821T>C (INTS12)	ENSP00000396309.1:n.156+1821T>C
ENST00000420368.6:c.156+1821T>C (INTS12)	ENSP00000412317.2:n.156+1821T>C
ENST00000433009.1:c.156+1821T>C (INTS12)	ENSP00000396729.1:n.156+1821T>C
ENST00000451321.6:c.156+1821T>C (INTS12)	ENSP00000415433.2:n.156+1821T>C
ENST00000503746.5:c.156+1821T>C (INTS12)	ENSP00000423618.1:n.156+1821T>C
ENST00000510406.1:n.163-2159A>G (ARHGEF38)
ENST00000618810.4:c.156+1821T>C (INTS12)	ENSP00000481164.1:n.156+1821T>C
NM_001142471.1:c.156+1821T>C (INTS12)	NP_001135943.1:n.156+1821T>C
NM_020395.3:c.156+1821T>C (INTS12)	NP_065128.2:n.156+1821T>C
XM_005263148.3:c.156+1821T>C (INTS12)	XP_005263205.1:n.156+1821T>C
XM_011532143.1:c.156+1821T>C (INTS12)	XP_011530445.1:n.156+1821T>C
XM_011532144.1:c.156+1821T>C (INTS12)	XP_011530446.1:n.156+1821T>C
XM_011532145.1:c.156+1821T>C (INTS12)	XP_011530447.1:n.156+1821T>C
XR_938768.1:n.419+1821T>C (INTS12)
XM_005263148.5:c.156+1821T>C (INTS12)	XP_005263205.1:n.156+1821T>C
XM_011532143.2:c.156+1821T>C (INTS12)	XP_011530445.1:n.156+1821T>C
XM_011532145.2:c.156+1821T>C (INTS12)	XP_011530447.1:n.156+1821T>C
XR_001741293.1:n.412+1821T>C (INTS12)
XR_001741294.1:n.253+1821T>C (INTS12)
NM_020395.4:c.156+1821T>C (INTS12) MANE Select	NP_065128.2:n.156+1821T>C
NM_001142471.2:c.156+1821T>C (INTS12)	NP_001135943.1:n.156+1821T>C