Canonical Allele Identifier: CA2676572666

Gene: MSX2

Linked Data

• gnomAD v4: 5-174724592-A-AGTCGG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.174724594_174724595insCGGGT , CM000667.2:g.174724594_174724595insCGGGT	GRCh38
NC_000005.9:g.174151597_174151598insCGGGT , CM000667.1:g.174151597_174151598insCGGGT	GRCh37
NC_000005.8:g.174084203_174084204insCGGGT	NCBI36
NG_008124.1:g.5023_5024insCGGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239243.7:c.-66_-65insCGGGT MANE Select	ENSP00000239243.5:n.-66_-65insCGGGT
ENST00000239243.6:c.-66_-65insCGGGT	ENSP00000239243.5:n.-66_-65insCGGGT
NM_002449.4:c.-66_-65insCGGGT	NP_002440.2:n.-66_-65insCGGGT
NM_001363626.1:c.-66_-65insCGGGT	NP_001350555.1:n.-66_-65insCGGGT
NM_002449.5:c.-66_-65insCGGGT MANE Select	NP_002440.2:n.-66_-65insCGGGT
NM_001363626.2:c.-66_-65insCGGGT	NP_001350555.1:n.-66_-65insCGGGT