Canonical Allele Identifier: CA657538010

Gene: MC2R

Linked Data

• COSMIC: COSN20079182

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.13885556_13885557insG , CM000680.2:g.13885556_13885557insG	GRCh38
NC_000018.9:g.13885555_13885556insG , CM000680.1:g.13885555_13885556insG	GRCh37
NC_000018.8:g.13875555_13875556insG	NCBI36
NG_011819.1:g.34980_34981insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327606.4:c.-39_-38insC MANE Select	ENSP00000333821.2:n.-39_-38insC
ENST00000327606.3:c.-39_-38insC	ENSP00000333821.2:n.-39_-38insC
ENST00000399821.2:c.-39_-38insC	ENSP00000382718.2:n.-39_-38insC
NM_000529.2:c.-39_-38insC MANE Select	NP_000520.1:n.-39_-38insC
NM_001291911.1:c.-39_-38insC	NP_001278840.1:n.-39_-38insC
XM_017025781.1:c.-39_-38insC	XP_016881270.1:n.-39_-38insC